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Looking for Tablet? Find Direct Compression & other pharma excipients for Tablet dosage forms on PharmaCompass.

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01 Aluminum Hydroxide Excipient (1)

02 Anhydrous Lactose (2)

03 Calcium Carbonate Excipient (4)

04 Carbomer Homopolymer Type A (1)

05 Croscarmellose Sodium (1)

06 Crospovidone (2)

07 Dibasic Calcium Phosphate (1)

08 Fructose (1)

09 Hydrogenated Castor Oil (1)

10 Hydroxypropyl Methylcellulose (1)

11 Lactose Monohydrate (7)

12 Lauryl Sulfate (1)

13 Magnesium Aluminometasilicate (1)

14 Magnesium aluminium silicate Excipient (1)

15 Maltose Sugar (1)

16 Mannitol (7)

17 Microcrystalline Cellulose (7)

18 Microprilled Poloxamer (2)

19 Native & Pregelatinized Corn Starch (1)

20 Polacrilin Potassium (1)

21 Polyethylene Oxide (1)

22 Polyoxyl 40 hydrogenated castor oil (1)

23 Polysorbate 80 (1)

24 Polyvinylpyrrolidone Crosslinked (4)

25 Polyvinylpyrrolidone and Vinyl Acetate Copolymer (1)

26 Povidone (2)

27 Simethicone Excipient (1)

28 Sodium Lauryl Sulfate (1)

29 Sodium Starch Glycolate (1)

30 Starch (1)

31 Stearic Acid (1)

32 Stearyl Alcohol (1)

33 Talc Excipient (1)

34 Vinylpyrrolidone-Vinyl Acetate (1)

35 Vinylpyrrolidone-Vinyl Acetate Copolymer (1)

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01 SPI Pharma (14)

02 DKSH (1)

03 Gangwal Healthcare (6)

04 Boai NKY Pharmaceuticals Ltd (1)

05 Alcedo Pharmachem (1)

06 BASF (15)

07 Corel Pharma Chem (1)

08 DFE Pharma (2)

09 Gangwal Chemicals (4)

10 Lubrizol Life Science Health (1)

11 Microlex e.U (6)

12 Prachin Chemical (1)

13 Seppic (3)

14 Sigachi Industries (5)

15 The Dow Chemical Company (1)

16 Ulanqab Kema New Material (1)

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01 Austria (6)

02 China (2)

03 France (3)

04 Germany (17)

05 India (18)

06 Switzerland (1)

07 U.S.A (16)

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CSP

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Applications:

Crospovidone is an insoluble polymer of N-vinyl-2-pyrrolidone that is used as a disintegrant in pharmaceutical tablets.

Ingredient(s): Crospovidone

Dosage Form: Tablet

Category: Direct Compression

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

Technical Specifications: NA

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Applications:

Pharmacel® 102 has good flow properties enabling high speed direct compression tableting. It is a ideal choice for direct compression & dry granulation formulations and it also has some lubrication properties for smooth tableting experience.

Ingredient(s): Microcrystalline Cellulose

Dosage Form: Tablet

Category: Direct Compression

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Conforms to USP-NF, Ph.Eur., JP, IP

Technical Specifications: Density- Tapped density- 440 g/l, Bulk density- 310 g/l; Particle size- D10- 40 ?m, D50- 90 ?m, D90-180 ?m; Hausner ratio-1,42

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ACECEL

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LM Application #LearnMore

Applications:

AceCel is suitable for majority of the directly compressible actives, combines good flow and high compressibility.

Ingredient(s): Microcrystalline Cellulose

Dosage Form: Tablet

Category: Direct Compression

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

Technical Specifications: Not Available

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HICEL

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Applications:

HiCel acts as a strong & dry binder. It facilitates low tablet friability & promotes rapid tablet disintegration.

Ingredient(s): Microcrystalline Cellulose

Dosage Form: Tablet

Category: Direct Compression

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

Technical Specifications: Not Available

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Applications:

SuperTab® 11SD offers the best compactability of all grades of lactose, and it is well suited to direct compression applications. Due to the low moisture content, it is used in the formulations containing moisture sensitive drugs.

Ingredient(s): Anhydrous Lactose

Dosage Form: Tablet

Category: Direct Compression

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Conforms to Ph. Eur., Lactose monograph / USP-NF, JP Anhydrous lactose monograph

Technical Specifications: Density- Tapped density- 906 g/l, Bulk density- 722 g/l; Particle size- D10-15 ?m, D50- 170 ?m, D90- 340 ?m; Hausner ratio-1,25

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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: Direct Compression

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

Technical Specifications: Not Available

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Applications:

Wetting agent, reducing disintegration time, direct compression, Hydrophilic lubricant, effervescent tablets.

Ingredient(s): Sodium Lauryl Sulfate

Dosage Form: Tablet

Category: Direct Compression

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Ph. Eur.: Sodium Laurilsulfate; USP-NF, JP: Sodium Lauryl Sulfate

Technical Specifications: Not Available

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Applications:

Tablets made from these granules are typically easily disintegrated using conventional super disintegrates even when hard tablets are compressed.

Ingredient(s): Microcrystalline Cellulose

Dosage Form: Tablet

Category: Direct Compression

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Monograph- USP/NF, JP/JPE

Technical Specifications: Not Available

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HICEL SMCC

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LM Application #LearnMore

Applications:

HiCel SMCC has unique combination which result in optimum compaction & superior flow properties.

Ingredient(s): Microcrystalline Cellulose, Silicon Dioxide

Dosage Form: Tablet

Category: Direct Compression

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

Technical Specifications: Not Available

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Applications:

Lactose monohydrate is typically used for wet or dry granulation. During wet granulation, liquid binders or adhesives are added to the lactose and active mixture, usually by blending.

Ingredient(s): Lactose Monohydrate

Dosage Form: Tablet

Category: Direct Compression

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Monograph- USP/NF, JP/JPE

Technical Specifications: Milled; Also Available as Microlex® LCM 180.m, Microlex® LCM 200.m

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Applications:

It is also suitable for both wet granulation and direct compression methods of tablet production. Microlex® crystalline grades are used in wet granulation and the spray dried forms are used in direct compression.

Ingredient(s): Lactose Monohydrate

Dosage Form: Tablet

Category: Direct Compression

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Monograph- USP/NF, JP/JPE

Technical Specifications: Sieved; Also Available as Microlex® LCM 180.s, Microlex® LCM 220.s

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Applications:

It is also suitable for both wet granulation and direct compression methods of tablet production. Microlex® crystalline grades are used in wet granulation and the spray dried forms are used in direct compression.

Ingredient(s): Anhydrous Lactose

Dosage Form: Tablet

Category: Direct Compression

Route of Administration (Grade): Oral
Pharmacopoeia Reference: Monograph- USP/NF, JP/JPE

Technical Specifications: Milled; Also Available as Microlex® LCA 120.m, Microlex® LCA 200.m

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FILLERLAC

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LM Application #LearnMore

Applications:

Lactose is widely used as a filler and diluent in tablets and capsules, and to a more limited extent in lyophilized products and infant formulas.

Ingredient(s): Lactose Monohydrate

Dosage Form: Tablet

Category: Direct Compression

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

Technical Specifications: Not Available

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Applications:

Carbopol® 71G NF polymer is widely used in oral solid dose applications.The unique feature of this polymer is its granular form due to which it is used in direct compression formulations. The residual solvent in Carbopol 71G NF is Ethyl acetate.

Ingredient(s): Carbomer Homopolymer Type A

Dosage Form: Tablet

Category: Direct Compression

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:

Use in a wide range of oral applications such as wet or dry granulation, excipient of choice for flash release forms.

Ingredient(s): Mannitol

Dosage Form: Tablet

Category: Direct Compression

Route of Administration (Grade): Topical, Oral
Pharmacopoeia Reference: Monograph- Ph.Eur, USP/NF

Technical Specifications: Available in different particle size as 25.µ, 50.µ, 180.µ

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Applications:

Lipophilic lubricant, for sensitive acidic APIs, sustained release melt coating. Used as consistency factor to enhance the viscosity of topical formulations.

Ingredient(s): Hydrogenated Castor Oil

Dosage Form: Tablet

Category: Direct Compression

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Ph. Eur., Castor Oil, hydrogenated, USP-NF: Hydrogenated Castor Oil, JP: Hydrogenated Oil

Technical Specifications: Not Available

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Applications:

Lipophilic lubricant, for sensitive acidic APIs, Structure-building consistency factor for semi-solids, Viscosity regulator.

Ingredient(s): Stearyl Alcohol

Dosage Form: Tablet

Category: Direct Compression

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

Technical Specifications: Not Available

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Applications:

Ready-to-use direct compression solution for tablets.

Ingredient(s): Crospovidone, Lactose, Povidone

Dosage Form: Tablet

Category: Direct Compression

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

Technical Specifications: Not Available

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Applications:

Ready-to-use direct compression solution for lozenges, chewables and effervescent tablets.

Ingredient(s): Lactose, Povidone

Dosage Form: Tablet

Category: Direct Compression

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Ph. Eur., USP/NF and J.P

Technical Specifications: Not Available

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Applications:

Wet Granulation and Direct Compression

Ingredient(s): Polacrilin Potassium, Sodium Polystyrene Sulphonate Excipient

Dosage Form: Tablet

Category: Direct Compression

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

Technical Specifications: Not Available

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Applications:

Capsule Filling, Direct Compression, Binding, Disintegration

Ingredient(s): Native & Pregelatinized Corn Starch

Dosage Form: Tablet

Category: Direct Compression

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

Technical Specifications: EXCiPACT

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Applications:

Solubilizer

Ingredient(s): Polyoxyl 40 hydrogenated castor oil

Dosage Form: Tablet

Category: Direct Compression

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

Technical Specifications: Solubilizer in powder form; EXCiPACT

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Applications:

Solubilizer

Ingredient(s): Polysorbate 80, Polysorbate 80

Dosage Form: Tablet

Category: Direct Compression

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

Technical Specifications: Solubilizer in powder form; EXCiPACT

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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: Direct Compression

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

Technical Specifications: Not Available

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Applications:

Fujicalin SG is a pharmaceutical excipient that acts as a diluent, filler and cushioning agent.

Ingredient(s): Dibasic Calcium Phosphate

Dosage Form: Tablet

Category: Direct Compression

Route of Administration (Grade): Oral
Pharmacopoeia Reference: USP-NF, EP, JPC, US DMF Type IV, Listed as GRAS

Technical Specifications: Not Available

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Applications:

Maximum disintegration

Ingredient(s): Polyvinylpyrrolidone Crosslinked

Dosage Form: Tablet

Category: Direct Compression

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

Technical Specifications: Not Available

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Applications:

Polysorbate 80 in dry powder form, a solubilizing agent acts as a surfactant and increases the solubility of various oral dosage forms.

Ingredient(s): Magnesium aluminium silicate Excipient, Polysorbate 80

Dosage Form: Tablet

Category: Direct Compression

Route of Administration (Grade): Oral
Pharmacopoeia Reference: USP-NF, EP, JP & having US DMF

Technical Specifications: Solubilizer in powder form, used in directly compressible dosage forms, Wet granulation, added during lubrication stage

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Applications:

Roller compaction & direct compression including slight disintegration functionality, Reduces sedimentation in suspensions. Solubilizer in transdermal patches.

Ingredient(s): Polyvinylpyrrolidone Crosslinked

Dosage Form: Tablet

Category: Direct Compression

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

Technical Specifications: Not Available

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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: Direct Compression

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:

Polyoxyl 40 hydrogenated castor oil is used as solubilizer and emulsifying agent.

Ingredient(s): Magnesium Aluminometasilicate, Polyoxyl 40 Hydrogenated Castor Oil

Dosage Form: Tablet

Category: Direct Compression

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

Technical Specifications: Solubilizer in powder form, used in Directly compressible dosage forms, Wet granulation, added during lubrication stage

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Applications:

Dry binder in tablets, capsules and granules, as a film-forming agent in tablet coatings and subcoatings, and as a film-forming agent in topical sprays. Widely used in HME processes.

Ingredient(s): Vinylpyrrolidone-Vinyl Acetate

Dosage Form: Tablet

Category: Direct Compression

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Ph. Eur., USP monograph "Copovidone" and the JPE monograph "Copolyvidone"

Technical Specifications: Not Available

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Applications:

Binder with fine particle size for roller compaction & direct compression

Ingredient(s): Vinylpyrrolidone-Vinyl Acetate Copolymer

Dosage Form: Tablet

Category: Direct Compression

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Ph. Eur., USP monograph "Copovidone" and the JPE monograph "Copolyvidone"

Technical Specifications: Not Available

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Applications:

Dissolution enhancer, lubricant & wetting agent, Hydrophilic lubricant, effervescent tablets.

Ingredient(s): Microprilled Poloxamer

Dosage Form: Tablet

Category: Direct Compression

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Ph. Eur., USP-NF: Poloxamer 188; JPE: Polyoxyethylene (160) Polyoxypropylene (30) glycol

Technical Specifications: Not Available

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Applications:

Dissolution enhancer, lubricant & wetting agent, Hydrophilic lubricant, effervescent tablets.

Ingredient(s): Microprilled Poloxamer

Dosage Form: Tablet

Category: Direct Compression

Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Ph. Eur., USP-NF: Poloxamer 407; JPE: Polyoxyethylene (196) Polyoxypropylene (67) glyco

Technical Specifications: Not Available

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Applications:

Kollidon CL-F has a balance of strong disintegration and optimal surface homogeneity.

Ingredient(s): Polyvinylpyrrolidone Crosslinked

Dosage Form: Tablet

Category: Direct Compression

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

Technical Specifications: Not Available

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