01 DKSH (6)
02 Evonik (16)
03 Gangwal Healthcare (5)
04 Boai NKY Pharmaceuticals Ltd (1)
05 Actylis (13)
06 Aeon Procare (4)
07 Alcedo Pharmachem (4)
08 BASF (35)
09 Corel Pharma Chem (20)
10 Finar (4)
11 Gangwal Chemicals (3)
12 Huzhou Sunflower Pharmaceutical Co. Ltd (1)
13 Ideal Cures Pvt Ltd (7)
14 Kerry (19)
15 Kima Chemical (1)
16 Lonza Capsugel (1)
17 Lubrizol Life Science Health (4)
18 Nomisma Healthcare (5)
19 Sigachi Industries (1)
20 The Dow Chemical Company (4)
21 Vertellus (14)
01 Capsule (43)
02 Emulsion (1)
03 Gel (1)
04 Granule / Pellet (12)
05 Softgel Capsule (5)
06 Solution (1)
07 Tablet (91)
08 Topical Film (3)
09 Transdermal Patch (11)
01 China (3)
02 Germany (51)
03 India (53)
04 Switzerland (6)
05 U.S.A (55)
Applications:
Ingredient(s): Sodium Alginate Excipient
Dosage Form: Tablet
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Ingredient(s): Alginic Acid
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Ingredient(s): Methacrylic Acid - Ethyl Acrylate Copolymer
Category: Controlled & Modified Release
Technical Specifications: Available as powder; Other grades- EUDRAGIT® L 30 D-55
Applications:
Ingredient(s): Microcrystalline Cellulose
Dosage Form: Capsule, Granule / Pellet, Tablet
Category: Controlled & Modified Release
Technical Specifications: NA
Applications:
Ingredient(s): Methyl Vinyl Ether and Maleic Anhydride Copolymer
Dosage Form: Gel
Category: Controlled & Modified Release
Technical Specifications: NA
Applications:
Ingredient(s): PLASACRYL T20
Category: Controlled & Modified Release
Technical Specifications: NA
Applications:
Ingredient(s): Gadolinium Oxide
Dosage Form: Tablet
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Ingredient(s): Ammonia Methacrylate Copolymer Type A
Category: Controlled & Modified Release
Technical Specifications: Other grades- EUDRAGIT® RL 12,5, EUDRAGIT® RL 30 D, EUDRAGIT® RL PO
Applications:
Ingredient(s): Talc Excipient
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Ingredient(s): PLASACRYL HTP20
Category: Controlled & Modified Release
Technical Specifications: NA
Applications:
Ingredient(s): EthylCellulose, Hydroxypropyl Cellulose, Hydroxypropyl Methylcellulose, Magnesium Stearate, Maize Starch, Microcrystalline Cellulose, Silicon Dioxide, Talc
Category: Controlled & Modified Release
Technical Specifications: NA
Applications:
Ingredient(s): Ammonio Methacrylate Copolymer Type B
Category: Controlled & Modified Release
Technical Specifications: Available as granules; Other grades- EUDRAGIT® RS 12,5, EUDRAGIT® RS 30 D, EUDRAGIT® RS PO
Applications:
Ingredient(s): Amino Methacrylate Copolymer
Category: Controlled & Modified Release
Technical Specifications: Available as granules; Other grades- EUDRAGIT® E 12,5, EUDRAGIT® E PO.
Applications:
Ingredient(s): Methacrylic Acid Copolymer Type B
Category: Controlled & Modified Release
Technical Specifications: Available as powder; Other grades- EUDRAGIT® S 12,5
Applications:
Ingredient(s): METHACRYLIC ACID COPOLYMER TYPE A
Category: Controlled & Modified Release
Technical Specifications: Available as powder; Other grades- EUDRAGIT® L 12,5
Applications:
Ingredient(s): Hydrated Silica, Lauryl Sulfate, Polyvinyl Acetate, Povidone
Dosage Form: Capsule, Tablet, Topical Film, Transdermal Patch
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Ingredient(s): Poly L Lactide, Polyethylene Glycol Excipient
Dosage Form: Tablet
Category: Controlled & Modified Release
Technical Specifications: Nano-particles, ultrapure, low-monomer & powder grades
Applications:
Ingredient(s): Hydroxypropyl Methylcellulose
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Ingredient(s): Methacrylic Acid - Ethyl Acrylate Copolymer
Dosage Form: Tablet
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Ingredient(s): Copovidone K25-31
Dosage Form: Tablet
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Ingredient(s): Talc Excipient
Dosage Form: Granule / Pellet, Tablet
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Ingredient(s): EthylCellulose
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Ingredient(s): Poly-DL-Lactic-co-Glycolic Acid, Polyethylene Glycol Excipients
Dosage Form: Tablet
Category: Controlled & Modified Release
Technical Specifications: Nano-particles, ultrapure, low-monomer & powder grades.
Applications:
Ingredient(s): Acetyl Triethyl Citrate
Dosage Form: Capsule, Granule / Pellet, Tablet
Category: Controlled & Modified Release
Technical Specifications: Slightly water soluble
Applications:
Ingredient(s): Methacrylic Acid Methyl Methacrylate Copolymer
Dosage Form: Tablet
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Ingredient(s): Poly L Lactide
Dosage Form: Tablet
Category: Controlled & Modified Release
Technical Specifications: Nano-particles, ultrapure, low-monomer & powder grades, viscosity range from 0.08 to 1.4 dL/g, ester/acid end group
Applications:
Ingredient(s): Methacrylic Acid - Ethyl Acrylate Copolymer
Dosage Form: Tablet
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Sustained Release Tablet Matrix
Ingredient(s): Hydroxypropyl Methylcellulose
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Kaolin is a naturally occurring mineral used in oral and topical pharmaceutical formulations
Ingredient(s): Kaolin Excipient
Dosage Form: Tablet, Transdermal Patch
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Ingredient(s): Poly DL Lactide
Dosage Form: Tablet
Category: Controlled & Modified Release
Technical Specifications: Nano-particles, ultrapure, low-monomer & powder grades, viscosity range from 0.08 to 1.4 dL/g, ester/acid end group
Applications:
A&C’s Acetone NF meets the USP-NF monograph.
Ingredient(s): Acetone Excipient
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Ingredient(s): Methacrylic Acid Methyl Methacrylate Copolymer
Dosage Form: Tablet
Category: Controlled & Modified Release
Technical Specifications: Not Available
Ingredient(s): polyethylene glycol
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Ingredient(s): Poly DL Lactide co Glycolide
Dosage Form: Tablet
Category: Controlled & Modified Release
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.
Applications:
Ingredient(s): Microcrystalline Cellulose
Dosage Form: Tablet
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Instamodel Blend is used to provide Extended Release from the dosage form.
Ingredient(s): HPMC 2910
Dosage Form: Tablet
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Ingredient(s): Microcrystalline Cellulose
Dosage Form: Tablet
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Ingredient(s): Tri-n-butyl Citrate
Dosage Form: Capsule, Granule / Pellet, Tablet
Category: Controlled & Modified Release
Technical Specifications: Water insoluble
Applications:
Ingredient(s): Hydroxypropyl Methylcellulose, Starch
Dosage Form: Tablet
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Ingredient(s): Hydrogenated Castor Oil
Category: Controlled & Modified Release
Technical Specifications: NA
Applications:
Ingredient(s): Sodium Alginate Excipient
Dosage Form: Tablet
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Hydroxypropyl Methyl Cellulose (75K100) is used in the production of controlled-release tablets.
Ingredient(s): Hydroxypropyl Methyl Cellulose
Dosage Form: Tablet
Category: Controlled & Modified Release
Technical Specifications: NA
Applications:
Ingredient(s): Hydroxypropyl Methylcellulose
Dosage Form: Tablet
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Ingredient(s): Hydroxypropyl Methylcellulose
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Ingredient(s): Hydroxypropyl Methylcellulose
Dosage Form: Tablet
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Ingredient(s): Methacrylic Acid - Ethyl Acrylate Copolymer
Category: Controlled & Modified Release
Technical Specifications: NA
Applications:
Ingredient(s): Hydroxypropyl Methylcellulose, Lactose
Dosage Form: Tablet
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Ingredient(s): Acetyl tri-n-butyl citrate
Dosage Form: Capsule, Granule / Pellet, Tablet
Category: Controlled & Modified Release
Technical Specifications: Water insoluble
Ingredient(s): Potassium Chloride Excipient
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Ingredient(s): Polyvinyl Alcohol
Dosage Form: Tablet
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Ingredient(s): Hydroxypropyl Methylcellulose
Dosage Form: Tablet
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Ingredient(s): HPMC AS, Hydroxypropyl Methyl Cellulose
Dosage Form: Capsule
Category: Controlled & Modified Release
Technical Specifications: Water content – less than 6%; Size #0
Applications:
Ingredient(s): Glycerol, Unmodified, Hydroxypropyl Methylcellulose
Dosage Form: Tablet
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
A & C's Phenyl Ethyl alcohol is a preservative that meets USP-NF and JP monographs.
Ingredient(s): Phenylethyl Alcohol Excipient
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Controlled-release coatings for tablets & capsules.
Ingredient(s): Dibutyl Sebacate
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
A & C's Phenyl Ethyl alcohol is an excipient which meets the USP monograph.
Ingredient(s): Phenylethyl Alcohol Excipient
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Ingredient(s): Carbomer Homopolymer Type A
Dosage Form: Tablet
Category: Controlled & Modified Release
Technical Specifications: Viscosity, cP (0.5 wt% at pH 7.5)- 4,000 - 11,000
Applications:
Ingredient(s): Hydroxypropyl Methylcellulose, Polydextrose Sugar
Dosage Form: Tablet
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Ingredient(s): Triethyl Citrate
Dosage Form: Capsule, Granule / Pellet, Tablet
Category: Controlled & Modified Release
Technical Specifications: Water soluble
Applications:
Ingredient(s): hydroxypropyl methylcellulose phthalate
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Ingredient(s): Carbomer Homopolymer Type B
Dosage Form: Tablet
Category: Controlled & Modified Release
Technical Specifications: Viscosity, cP (0.5 wt% at pH 7.5)- 29,400 - 39,400
Applications:
Ingredient(s): Polycarbophil
Category: Controlled & Modified Release
Technical Specifications: Viscosity, cP (0.2 wt% at pH 7.5) - 2,000 - 12,000
Applications:
Solvent for injectables and oral formulations for animal health
Ingredient(s): Pyrrolidone
Dosage Form: Emulsion
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Enteric, Delayed Release Matrix and Solubility Enhancement
Ingredient(s): Methacrylic Acid - Ethyl Acrylate Copolymer
Category: Controlled & Modified Release
Technical Specifications: Methylacryli acid and Ethyl Acrylate copolymer (1:1) Type A
Applications:
Ingredient(s): Acrylate copolymer
Dosage Form: Tablet
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
A & C's Sodium Citrate Dihydrate multi-compendial is a trisodium salt of citric acid.
Ingredient(s): Sodium Citrate Dihydrate Excipient
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Ingredient(s): EthylCellulose, Hydroxypropyl Methylcellulose
Dosage Form: Tablet
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
A & C's Sodium Citrate Dihydrate USP-NF is a trisodium salt of citric acid.
Ingredient(s): Sodium Citrate Dihydrate Excipient
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
A&C's Sodium Hydroxide is a highly caustic concentrate solution.
Ingredient(s): Sodium Hydroxide Excipient
Category: Controlled & Modified Release
Technical Specifications: Solution 50% (w/w)
Applications:
Ingredient(s): Lecithin, Polyvinyl Alcohol
Dosage Form: Tablet
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Sustained Release (Insoluble & High Permeability)
Ingredient(s): Ammonia Methacrylate Copolymer Type A
Dosage Form: Tablet, Transdermal Patch
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Ingredient(s): Hydroxypropyl Cellulose, Hydroxypropyl Methylcellulose
Dosage Form: Tablet
Category: Controlled & Modified Release
Technical Specifications: Not Available
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
Technical Specifications: Not Available
Applications:
Sustained Release (Insoluble & High Permeability)
Ingredient(s): Ammonia Methacrylate Copolymer Type A
Dosage Form: Tablet, Transdermal Patch
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Sustained release (Insoluble & Low Permeability)
Ingredient(s): Ammonio Methacrylate Copolymer Type B
Dosage Form: Tablet, Transdermal Patch
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Ingredient(s): Hydroxypropyl Methylcellulose, Polyvinyl Alcohol
Dosage Form: Tablet
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Sustained Release (Insoluble & High Permeability)
Ingredient(s): Ammonio Methacrylate Copolymer Type B
Dosage Form: Tablet, Transdermal Patch
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Sustained Release (Insoluble & High Permeability)
Ingredient(s): Ammonio Methacrylate Copolymer Type B
Dosage Form: Tablet, Transdermal Patch
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Ingredient(s): Carbomer Homopolymer Type A
Dosage Form: Tablet
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Ingredient(s): Carbomer Homopolymer Type A
Dosage Form: Tablet
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Ingredient(s): Carbomer Homopolymer Type A
Dosage Form: Tablet
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Ingredient(s): Carbomer 941
Dosage Form: Tablet
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Sustained Release, Taste Masking, Moisture Barrier, Binder in Wet Granulation
Ingredient(s): Ethyl Cellulose
Dosage Form: Capsule, Granule / Pellet, Tablet
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Ingredient(s): Hydrogenated Castor Oil
Dosage Form: Tablet
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Sustained Release (Insoluble & High Permeability)
Ingredient(s): Ammonio Methacrylate Copolymer
Dosage Form: Tablet, Transdermal Patch
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Ingredient(s): Methacrylic Acid & Ethyl Acrylate Copolymer
Dosage Form: Capsule, Granule / Pellet, Softgel Capsule, Tablet
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Enteric coating with release above pH 5.5 (partially preneutralized powder)
Ingredient(s): Methacrylic Acid & Ethyl Acrylate Copolymer
Dosage Form: Capsule, Granule / Pellet, Softgel Capsule, Tablet
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Enteric coating with release above pH 5.5 (30 % solids content dispersion)
Ingredient(s): Methacrylic Acid & Ethyl Acrylate Copolymer
Dosage Form: Capsule, Granule / Pellet, Softgel Capsule, Tablet
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Ingredient(s): Polyethylene Oxide
Dosage Form: Tablet
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Ingredient(s): Polyvinyl Acetate, Sodium Lauryl Sulfate
Dosage Form: Capsule, Granule / Pellet, Softgel Capsule, Tablet, Topical Film
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Solubilization, dispersion, crystallization inhibition, instant release matrices & spray drying
Ingredient(s): Povidone
Dosage Form: Capsule, Tablet, Transdermal Patch
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Solubilization, dispersion, crystallization inhibition, instant release matrices & spray drying
Ingredient(s): Povidone
Dosage Form: Capsule, Tablet, Transdermal Patch
Category: Controlled & Modified Release
Technical Specifications: Not Available
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: Capsule, Granule / Pellet, Softgel Capsule, Tablet
Category: Controlled & Modified Release
Technical Specifications: Not Available
Applications:
Solubility and bioavailability enhancement, ideal for hot melt extrusion (HME)
Ingredient(s): polyethylene glycol, Polyvinyl Acetate
Dosage Form: Tablet, Topical Film, Transdermal Patch
Category: Controlled & Modified Release
Technical Specifications: Not Available