Overview of Ethanol

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02882_FLUKA
  • Synopsis

  • Chemistry

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  • FDA
  • EDQM
Applications: Compressol® SM, co-processed polyol, is a directly compressible pharmaceutical excipient comprised of mannitol and sorbitol. It provides superior compactibility of sorbitol, while retaining lower hygroscopicity & a lower disintegration time.
Ingredient(s): Mannitol
Route of Administration (Grade): Oral
Pharmacopoeia Reference: Not Available
Technical Specifications: Not Available
  • WHO-GMP
Applications: Polysorbate 80 in dry powder form
Ingredient(s): Polysorbate 80
Dosage Form: Tablet, Capsule
Route of Administration (Grade): Solid 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
  • FDA
Applications: Standard Direct Tabletting
Ingredient(s): Mannitol
Dosage Form: Tablet
More Info on Category: Co-Processed Excipients
Route of Administration (Grade): Not Available
Pharmacopoeia Reference: NF/EP/JP
Technical Specifications: Not Available
  • WHO-GMP
Applications: Polyoxyl 40 hydrogenated castor oil In dry powder form
Dosage Form: Tablet, Capsule
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
  • FDA
Applications: Direct Compression
Dosage Form: Tablet
More Info on Category: Co-Processed Excipients
Route of Administration (Grade): Not Available
Pharmacopoeia Reference: NF/EP/JP
Technical Specifications: Not Available
  • FDA
Applications: Direct Compression
Dosage Form: Tablet
More Info on Category: Co-Processed Excipients
Route of Administration (Grade): Not Available
Pharmacopoeia Reference: NF/EP/JP
Technical Specifications: Not Available
  • FDA
Applications: Direct Compression
Ingredient(s): Anhydrous Lactose
Dosage Form: Tablet
More Info on Category: Co-Processed Excipients
Route of Administration (Grade): Not Available
Pharmacopoeia Reference: NF/EP/JP
Technical Specifications: Not Available
  • FDA
Applications: Standard Direct Tabletting Or Roller Compaction
Ingredient(s): Anhydrous Lactose
Dosage Form: Tablet
More Info on Category: Co-Processed Excipients
Route of Administration (Grade): Not Available
Pharmacopoeia Reference: NF/EP/JP
Technical Specifications: Not Available
  • FDA
Applications: Direct Tabletting Operations Where Fast Disintegration Is Required
Ingredient(s): Lactose
Dosage Form: Tablet
More Info on Category: Co-Processed Excipients
Route of Administration (Grade): Not Available
Pharmacopoeia Reference: NF/EP/JP
Technical Specifications: Not Available
  • FDA
Applications: Orally Disintegrating Tablets
Ingredient(s): Mannitol
Dosage Form: Tablet
More Info on Category: Co-Processed Excipients
Route of Administration (Grade): Not Available
Pharmacopoeia Reference: USP/NF
Technical Specifications: Not Available
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  • SOLUTION;INTRA-ARTERIAL - 99% (1ML)
  • SOLUTION;INTRA-ARTERIAL - 99% (5ML)
  • SOLUTION;TOPICAL - 61%;1%
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