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Looking for Tablet? Find Controlled & Modified Release & other pharma excipients for Tablet dosage forms on PharmaCompass.

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01 Acetone Excipient (1)

02 Acetyl Triethyl Citrate (1)

03 Acetyl tri-n-butyl citrate (1)

04 Acrylate copolymer (1)

05 Alginic Acid (1)

06 Amino Methacrylate Copolymer (1)

07 Ammonia Methacrylate Copolymer Type A (3)

08 Ammonio Methacrylate Copolymer (1)

09 Ammonio Methacrylate Copolymer Type B (4)

10 Carbomer 941 (1)

11 Carbomer Homopolymer Type A (4)

12 Carbomer Homopolymer Type B (1)

13 Copovidone K25-31 (1)

14 Dibutyl Sebacate (1)

15 Ethyl Cellulose (1)

16 EthylCellulose (3)

17 Gadolinium Oxide (1)

18 HPMC 2910 (1)

19 Hydrogenated Castor Oil (2)

20 Hydroxypropyl Methyl Cellulose (1)

21 Hydroxypropyl Methylcellulose (9)

22 Kaolin Excipient (1)

23 Lauryl Sulfate (1)

24 METHACRYLIC ACID COPOLYMER TYPE A (1)

25 Methacrylic Acid & Ethyl Acrylate Copolymer (3)

26 Methacrylic Acid - Ethyl Acrylate Copolymer (5)

27 Methacrylic Acid Copolymer Type B (1)

28 Methacrylic Acid Methyl Methacrylate Copolymer (2)

29 Microcrystalline Cellulose (3)

30 PLASACRYL HTP20 (1)

31 PLASACRYL T20 (1)

32 Phenylethyl Alcohol Excipient (2)

33 Poly DL Lactide (1)

34 Poly DL Lactide co Glycolide (1)

35 Poly L Lactide (2)

36 Poly-DL-Lactic-co-Glycolic Acid (1)

37 Polycarbophil (1)

38 Polydextrose Sugar (1)

39 Polyethylene Oxide (1)

40 Polyvinyl Acetate (1)

41 Polyvinyl Alcohol (3)

42 Polyvinyl Alcohol Graft Polyethylene Glycol Copolymer (1)

43 Potassium Chloride Excipient (1)

44 Povidone (2)

45 Sodium Alginate Excipient (2)

46 Sodium Citrate Dihydrate Excipient (2)

47 Sodium Hydroxide Excipient (1)

48 Starch (1)

49 Talc Excipient (2)

50 Tri-n-butyl Citrate (1)

51 Triethyl Citrate (1)

52 Xylitol Excipient (1)

53 hydroxypropyl methylcellulose phthalate (1)

54 polyethylene glycol (2)

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01 DKSH (4)

02 Evonik (8)

03 Gangwal Healthcare (2)

04 Actylis (7)

05 Aeon Procare (2)

06 Alcedo Pharmachem (2)

07 BASF (9)

08 Corel Pharma Chem (12)

09 Finar (2)

10 Gangwal Chemicals (2)

11 Huzhou Sunflower Pharmaceutical Co. Ltd (1)

12 Ideal Cures Pvt Ltd (7)

13 Kerry (16)

14 Kima Chemical (1)

15 Lubrizol Life Science Health (3)

16 Nomisma Healthcare (5)

17 Sigachi Industries (1)

18 The Dow Chemical Company (2)

19 Vertellus (5)

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01 China (2)

02 Germany (17)

03 India (35)

04 Switzerland (4)

05 U.S.A (33)

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Applications:

For non-erodible matrices using direct compression, Controlled release matrix. Matrix former in transdermal patches and topical films.

Ingredient(s): Hydrated Silica, Lauryl Sulfate, Polyvinyl Acetate, Povidone

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Ph. Eur., USP-NF, JP-JPE: 80 % Polyvinyl acetate and 19 % povidone, 0.8 % lauryl sulfate & 0.2 % silica (4:1)

Technical Specifications: Not Available

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Applications:

PLLA-PEG used in the synthesis of targeted nanoparticles which are used for differential delivery and controlled release of drugs.

Ingredient(s): Poly L Lactide, Polyethylene Glycol Excipient

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Oral, Parenteral
Pharmacopoeia Reference: NA

Technical Specifications: Nano-particles, ultrapure, low-monomer & powder grades

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TALC

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Applications:

Talc is a widely used as a dissolution retardant in the development of controlled release products. Talc is also used as a lubricant in tablet formulations.

Ingredient(s): Talc Excipient

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Oral & Topical
Pharmacopoeia Reference: Not Available

Technical Specifications: Not Available

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Applications:

PLGA-PEG is used in the synthesis of targeted nanoparticles which are used for differential delivery and controlled release of drugs.

Ingredient(s): Poly-DL-Lactic-co-Glycolic Acid, Polyethylene Glycol Excipients

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Oral, Parenteral
Pharmacopoeia Reference: NA

Technical Specifications: Nano-particles, ultrapure, low-monomer & powder grades.

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Applications:

Sustained Release Tablet Matrix

Ingredient(s): Hydroxypropyl Methylcellulose

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: USP, EP, and JP

Technical Specifications: Not Available

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PLLA

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Applications:

PLLA (Poly-L-lactide) is different polymer developed to formulate polymeric nanoparticles. PLLA is biodegradable & biocompatible, and it is approved by FDA and European Medicine Agency for parenteral administration.

Ingredient(s): Poly L Lactide

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Oral, Parenteral
Pharmacopoeia Reference: NA

Technical Specifications: Nano-particles, ultrapure, low-monomer & powder grades, viscosity range from 0.08 to 1.4 dL/g, ester/acid end group

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KAOLIN

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Applications:

Kaolin is a naturally occurring mineral used in oral and topical pharmaceutical formulations

Ingredient(s): Kaolin Excipient

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Topical & Oral
Pharmacopoeia Reference: Not Available

Technical Specifications: Not Available

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PDLLA

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Applications:

PDLLA (Poly-DL-lactide) is different polymers developed to formulate polymeric nanoparticles. PDLLA is biodegradable & biocompatible, and it has the FDA and EMA approval in drug delivery systems for parenteral administration.

Ingredient(s): Poly DL Lactide

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Oral, Parenteral
Pharmacopoeia Reference: NA

Technical Specifications: Nano-particles, ultrapure, low-monomer & powder grades, viscosity range from 0.08 to 1.4 dL/g, ester/acid end group

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POLYETHYLENE GLYCOL 400 NF

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Ingredient(s): polyethylene glycol

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Topical and Oral
Pharmacopoeia Reference: Not Available

Technical Specifications: Not Available

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ACETONE NF

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Applications:

A&C’s Acetone NF meets the USP-NF monograph.

Ingredient(s): Acetone Excipient

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Oral
Pharmacopoeia Reference: NF

Technical Specifications: Not Available

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PLGA

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Applications:

PLGA (Poly (Lactic-Co-Glycolic Acid)) is a unique base polymer for controlled release of drugs & medical implant materials. It is biodegradable & biocompatible and since both monomers occur naturally it has minimal toxicity.

Ingredient(s): Poly DL Lactide co Glycolide

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Oral, Parenteral
Pharmacopoeia Reference: NA

Technical Specifications: Nano-particles, ultrapure, low-monomer & powder grades, available ratio PLGA 50:50, PLGA 75:25, PLGA 85:15, PLGA 55:45 Star Glucose, PLGA 65:35, PLGA 90:10.

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Applications:

Instamodel Blend is used to provide Extended Release from the dosage form.

Ingredient(s): HPMC 2910

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Not Available

Technical Specifications: Not Available

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HICEL MCC SPHERES

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Applications:

HiCel MCC Spheres are extremely versatile which is used for controlled release or sustained release formulations.

Ingredient(s): Microcrystalline Cellulose

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Not Available

Technical Specifications: Not Available

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Applications:

Immediate Release

Ingredient(s): Hydroxypropyl Methylcellulose, Starch

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Customized per requirements

Technical Specifications: Not Available

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Applications:

Immediate Release

Ingredient(s): Hydroxypropyl Methylcellulose

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Customized per requirements

Technical Specifications: Not Available

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Applications:

Controlled Release, Direct Compression,Wet Granulation,Tablet Coating, Liquid Solutions and Suspensions

Ingredient(s): Hydroxypropyl Methylcellulose

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Not Available

Technical Specifications: Not Available

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Applications:

Immediate Release

Ingredient(s): Hydroxypropyl Methylcellulose

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Customized per requirements

Technical Specifications: Not Available

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Applications:

Immediate Release

Ingredient(s): Hydroxypropyl Methylcellulose, Lactose

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Customized per requirements

Technical Specifications: Not Available

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Applications:

Immediate Release

Ingredient(s): Polyvinyl Alcohol

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Customized per requirements

Technical Specifications: Not Available

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POTASSIUM CHLORIDE

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Ingredient(s): Potassium Chloride Excipient

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Parenteral
Pharmacopoeia Reference: Not Available

Technical Specifications: Not Available

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Applications:

Immediate Release

Ingredient(s): Hydroxypropyl Methylcellulose

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Customized per requirements

Technical Specifications: Not Available

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PHENYL ETHYL ALCOHOL MULTI-COMPENDIAL

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Applications:

A & C's Phenyl Ethyl alcohol is a preservative that meets USP-NF and JP monographs.

Ingredient(s): Phenylethyl Alcohol Excipient

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Multi-compendial

Technical Specifications: Not Available

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Applications:

Immediate Release

Ingredient(s): Glycerol, Unmodified, Hydroxypropyl Methylcellulose

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Customized per requirements

Technical Specifications: Not Available

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PHENYL ETHYL ALCOHOL USP

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Applications:

A & C's Phenyl Ethyl alcohol is an excipient which meets the USP monograph.

Ingredient(s): Phenylethyl Alcohol Excipient

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Oral
Pharmacopoeia Reference: USP

Technical Specifications: Not Available

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DIBUTYL SEBACATE

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Applications:

Controlled-release coatings for tablets & capsules.

Ingredient(s): Dibutyl Sebacate

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Oral
Pharmacopoeia Reference: NF

Technical Specifications: Not Available

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Applications:

Carbopol® 971P NF polymer is used in oral & mucosal contact applications such as extended/controlled release tablets, oral liquids, suspension & bioadhesive formulations. The residual solvent of Carbopol 971P NF is Ethyl acetate.

Ingredient(s): Carbomer Homopolymer Type A

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Oral & Topical
Pharmacopoeia Reference: United States Pharmacopeia/National Formulary (USP/NF) monograph for Carbomer Homopolymer Type A, European Pharmacopeia (Ph. Eur.), India Pharmacopeia (IP), China Pharmacopeia (ChP) monographs for Carbomers.

Technical Specifications: Viscosity, cP (0.5 wt% at pH 7.5)- 4,000 - 11,000

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Applications:

Immediate Release

Ingredient(s): Hydroxypropyl Methylcellulose, Polydextrose Sugar

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Customized per requirements

Technical Specifications: Not Available

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Applications:

Carbopol® 974P NF polymer is used in oral and mucosal contact applications such as oral liquids, bioadhesive formulations, & extended release tablets. Additionally, it can be used to formulate viscous gels, emulsions & suspensions.

Ingredient(s): Carbomer Homopolymer Type B

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Oral & Topical
Pharmacopoeia Reference: United States Pharmacopeia/National Formulary (USP/NF) monograph for Carbomer Homopolymer Type B, European Pharmacopeia (Ph. Eur.), India Pharmacopeia (IP), China Pharmacopeia (ChP) mongographs for Carbomers.

Technical Specifications: Viscosity, cP (0.5 wt% at pH 7.5)- 29,400 - 39,400

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Applications:

Noveon® polycarbophil provides excellent bioadhesive properties & can be used for the formulation of buccal, nasal, ophthalmic, rectal bioadhesive products. lt can also be used as a controlled release polymer in oral solid dose applications.

Ingredient(s): Polycarbophil

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Topical, Oral, Nasal & Ophthalmics
Pharmacopoeia Reference: United States Pharmacopeia/National Formulary (USP/NF) monograph for Polycarbophil.

Technical Specifications: Viscosity, cP (0.2 wt% at pH 7.5) - 2,000 - 12,000

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Applications:

Enteric, Delayed Release Matrix and Solubility Enhancement

Ingredient(s): Methacrylic Acid - Ethyl Acrylate Copolymer

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Multicompendial

Technical Specifications: Methylacryli acid and Ethyl Acrylate copolymer (1:1) Type A

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Applications:

Enteric Coatings

Ingredient(s): Acrylate copolymer

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Customized per requirements

Technical Specifications: Not Available

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SODIUM CITRATE DIHYDRATE MULTI-COMPENDIAL

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Applications:

A & C's Sodium Citrate Dihydrate multi-compendial is a trisodium salt of citric acid.

Ingredient(s): Sodium Citrate Dihydrate Excipient

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Multi-compendial

Technical Specifications: Not Available

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Applications:

Enteric Coatings

Ingredient(s): EthylCellulose, Hydroxypropyl Methylcellulose

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Customized per requirements

Technical Specifications: Not Available

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SODIUM CITRATE DIHYDRATE USP-NF

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Applications:

A & C's Sodium Citrate Dihydrate USP-NF is a trisodium salt of citric acid.

Ingredient(s): Sodium Citrate Dihydrate Excipient

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Oral
Pharmacopoeia Reference: USP/NF

Technical Specifications: Not Available

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SODIUM HYDROXIDE NF

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Applications:

A&C's Sodium Hydroxide is a highly caustic concentrate solution.

Ingredient(s): Sodium Hydroxide Excipient

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Parenteral
Pharmacopoeia Reference: NF

Technical Specifications: Solution 50% (w/w)

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Applications:

Immediate Release

Ingredient(s): Lecithin, Polyvinyl Alcohol

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Customized per requirements

Technical Specifications: Not Available

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ACRYCOAT RL100

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Applications:

Sustained Release (Insoluble & High Permeability)

Ingredient(s): Ammonia Methacrylate Copolymer Type A

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Ph.Eur.: Ammonia Methacrylate Copolymer, Type A

Technical Specifications: Not Available

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Applications:

Immediate Release

Ingredient(s): Hydroxypropyl Cellulose, Hydroxypropyl Methylcellulose

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Customized per requirements

Technical Specifications: Not Available

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XYLITOL MULTI-COMPENDIAL

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Applications:

A & C's Xylitol multi-compendial is an excipient meeting USP-NF, EP and BP monographs.

Ingredient(s): Xylitol Excipient

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Multi-compendial

Technical Specifications: Not Available

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ACRYCOAT RLPO

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Applications:

Sustained Release (Insoluble & High Permeability)

Ingredient(s): Ammonia Methacrylate Copolymer Type A

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Oral & Topical
Pharmacopoeia Reference: USP/NF: Ammonia Methacrylate Copolymer, Type A - NF

Technical Specifications: Not Available

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Applications:

Immediate Release

Ingredient(s): Hydroxypropyl Methylcellulose, Polyvinyl Alcohol

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Customized per requirements

Technical Specifications: Not Available

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ACRYCOAT RS 30 D

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Applications:

Sustained release (Insoluble & Low Permeability)

Ingredient(s): Ammonio Methacrylate Copolymer Type B

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Oral and Topical
Pharmacopoeia Reference: Not Available

Technical Specifications: Not Available

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ACRYCOAT RS100

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Applications:

Sustained Release (Insoluble & High Permeability)

Ingredient(s): Ammonio Methacrylate Copolymer Type B

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Oral and Topical
Pharmacopoeia Reference: USP/NF: Ammonia Methacrylate Copolymer, Type B - NF

Technical Specifications: Not Available

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ACRYCOAT RSPO

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Applications:

Sustained Release (Insoluble & High Permeability)

Ingredient(s): Ammonio Methacrylate Copolymer Type B

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Oral and Topical
Pharmacopoeia Reference: USP/NF: Ammonia Methacrylate Copolymer, Type B - NF

Technical Specifications: Not Available

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ACRYPOL 971

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Applications:

It is widely used in oral solid, liquid dosage forms & topical formulations. It acts as excellent gel matrix former for controlling drug release in solid dosage forms.

Ingredient(s): Carbomer Homopolymer Type A

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Oral and Topical
Pharmacopoeia Reference: USP/NF : Carbomer Homopolymer Type A, EP : Carbomers

Technical Specifications: Not Available

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ACRYPOL 971G

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Applications:

It is widely used in oral solid, liquid dosage forms & topical formulations. It acts as excellent gel matrix former for controlling drug release in solid dosage forms.

Ingredient(s): Carbomer Homopolymer Type A

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Oral and Topical
Pharmacopoeia Reference: USP/NF: Carbomer Homopolymer Type A, EP : Carbomers

Technical Specifications: Not Available

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ACRYPOL 971P

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Applications:

It is widely used in oral solid, liquid dosage forms & topical formulations. It acts as excellent gel matrix former for controlling drug release in solid dosage forms.

Ingredient(s): Carbomer Homopolymer Type A

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Oral and Topical
Pharmacopoeia Reference: USP/NF : Carbomer Homopolymer Type A, EP : Carbomers

Technical Specifications: Not Available

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ACRYPOL 941

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Applications:

It is widely used in oral solid, liquid dosage forms & topical formulations. It acts as excellent gel matrix former for controlling drug release in solid dosage forms.

Ingredient(s): Carbomer 941

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Oral and Topical
Pharmacopoeia Reference: USP/NF : Carbomer 941

Technical Specifications: Not Available

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NUTRACOAT EC25D

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Applications:

Sustained Release, Taste Masking, Moisture Barrier, Binder in Wet Granulation

Ingredient(s): Ethyl Cellulose

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Oral
Pharmacopoeia Reference: USP/NF: Ethyl cellulose dispersion Type B

Technical Specifications: Not Available

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ACRYFLOW S

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Applications:

Lipophilic lubricant, Acryflow is used as an emulsifier for oil-in-water emulsions and as a pH independent sustained release agent. It acts as a plasticizer in solid dispersions.

Ingredient(s): Hydrogenated Castor Oil

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Oral and Topical
Pharmacopoeia Reference: USP/NF: Hydrogenated Castor Oil EP: Castor Oil, Hydrogenated

Technical Specifications: Not Available

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ACRYCOAT RL 30 D

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Applications:

Sustained Release (Insoluble & High Permeability)

Ingredient(s): Ammonio Methacrylate Copolymer

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Not Available

Technical Specifications: Not Available

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Applications:

Enteric coating with release above pH 5.5 (partially preneutralized powder)

Ingredient(s): Methacrylic Acid & Ethyl Acrylate Copolymer

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Ph. Eur.: Methacrylic Acid

Technical Specifications: Not Available

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Applications:

Enteric coating with release above pH 5.5 (30 % solids content dispersion)

Ingredient(s): Methacrylic Acid & Ethyl Acrylate Copolymer

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Ph. Eur.: Methacrylic Acid

Technical Specifications: Not Available

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Applications:

Peo-NF is a pharmaceutical excipient that acts as a diluent in osmotic tablets and sustained-release tablets.

Ingredient(s): Polyethylene Oxide

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Oral
Pharmacopoeia Reference: USP-NF

Technical Specifications: Not Available

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Applications:

pH-independent sustained release coating for small particles, pellets, granules and tablets. Sprayable polymeric film former. Flexible. Wash resistant.

Ingredient(s): Polyvinyl Acetate, Sodium Lauryl Sulfate

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Ph. Eur.: Poly(vinyl acetate) dispersion 30 per cent; USP: Polyvinyl Acetate Dispersion

Technical Specifications: Not Available

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Applications:

Solubilization, dispersion, crystallization inhibition, instant release matrices & spray drying

Ingredient(s): Povidone

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Ph. Eur., USP, JP

Technical Specifications: Not Available

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Applications:

Solubilization, dispersion, crystallization inhibition, instant release matrices & spray drying

Ingredient(s): Povidone

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Ph. Eur., USP, JP: Povidone

Technical Specifications: Not Available

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Applications:

Flexible water soluble instant release coating polymer, especially used for moisture protection

Ingredient(s): Polyvinyl Alcohol Graft Polyethylene Glycol Copolymer, Polyvinyl Alcohol

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Excipient based on Kollicoat® IR and monographed raw materials

Technical Specifications: Not Available

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Applications:

Solubility and bioavailability enhancement, ideal for hot melt extrusion (HME)

Ingredient(s): polyethylene glycol, Polyvinyl Acetate

Dosage Form: Tablet

Category: Controlled & Modified Release

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Polyvinyl caprolactam – polyvinyl acetate – polyethylene glycol graft copolymer

Technical Specifications: Not Available

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