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Overview of Alprazolam

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Alprox
  • Synopsis

  • Chemistry

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US DMFs Filed

US DMFs Filed

CEP/COS Certifications

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JDMFs Filed

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API REF. PRICE (USD / KG)
629

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USA (Orange Book)

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Europe

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Canada

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GLOBAL SALES (USD Million)

U.S. Medicaid

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EXCIPIENTS
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USFDA Orange Book Patents

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SERVICES

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  • FDA
Applications:
Ingredient(s): Sorbitol
Dosage Form: Tablet
More Info on Category: Taste Masking
Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Not Available
Technical Specifications: Not Available
  • FDA
  • EDQM
Applications: Sorbitol Special® is an effective plasticizer for soft gel formulations making the shell more pliable and robust. These grades reduce drying time, driving productivity and also enhance the gloss of the capsule for a premium appearance
Ingredient(s): Sorbitol
Dosage Form: Softgels
More Info on Category: Film Formers & Plasticizers
Route of Administration (Grade): Oral
Pharmacopoeia Reference: Not Available
Technical Specifications: Not Available
  • WHO-GMP
Applications: Ready mix Film coating system for moisture sensitive APIs
Ingredient(s): Stearic Acid
Dosage Form: Capsule, Tablet
Route of Administration (Grade): Oral
Pharmacopoeia Reference: USP / EP / JP; Having US-DMF
Technical Specifications: Moisture barrier film coating system
  • WHO-GMP
Applications: Ready mix Non-Functional film coating system.
Dosage Form: Capsule, Tablet
Route of Administration (Grade): Oral
Pharmacopoeia Reference: USP / EP / JP; Having US-DMF
Technical Specifications: Ready mix Non-Functional film coating system
  • WHO-GMP
Applications: Kovidone- K series products posses excellent binding, film-forming, dispersing, and thickning properties and are widely used in the following dosage forms. BinderSolubilizerCoating agentSuspending, Stabilizing or viscocity modifying agent
Ingredient(s): Polyvinylpyrrolidone
Dosage Form: Capsule, Tablet
Route of Administration (Grade): Solid Orals
Pharmacopoeia Reference: USP-NF/EP/BP/IP/JP/FCC
Technical Specifications: PVP K-K-30/ K-17/ K19/ K25/ K90
  • WHO-GMP
Applications: Polysorbates / TWEENs
Ingredient(s): Polysorbate 80
Route of Administration (Grade): Solid Oral, Liquid, Topical
Pharmacopoeia Reference: USP-NF / EP / JP
Technical Specifications: Non-Ionic Hydrophilic surfactant, Emulsifier (o/w emulsion), Solubilizer
  • FDA
  • EDQM
Applications: A natural inert polymer and ready-to-use coating system for fast aqueous film coating saves up to 50% or more time.
Dosage Form: Capsule, Tablet
Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Not Available
Technical Specifications: Not Available
    Applications: Tablet film coating, binders , main material of plant capsules.
    Ingredient(s): Hypromellose
    Dosage Form: Capsule, Tablet
    Route of Administration (Grade): Not Available
    Pharmacopoeia Reference: USP/BP/EP/CP
    Technical Specifications: Not Available
      Applications:
      Ingredient(s): Propylene Glycol
      More Info on Category: Film Formers & Plasticizers, Topical
      Route of Administration (Grade): Topical and Oral
      Pharmacopoeia Reference: Not Available
      Technical Specifications: Not Available
        Applications: The product is crystalline powder with sweet taste,odor free and humidizing. It is used in the chewing gum,candy,the sweetened bean paste,and so forth sugar free products. It is also used as raw material for Health products.
        Ingredient(s): Sorbitol
        Dosage Form: Syrup, Tablet
        More Info on Category: Taste Masking
        Route of Administration (Grade): Not Available
        Pharmacopoeia Reference: Not Available
        Technical Specifications: Pharma Grade/Food Grade
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        • TABLET;ORAL - 0.25MG
        • TABLET;ORAL - 0.5MG
        • TABLET;ORAL - 1MG
        • TABLET;ORAL - 2MG
        • TABLET, EXTENDED RELEASE;ORAL - 0.5MG
        • TABLET, EXTENDED RELEASE;ORAL - 1MG
        • TABLET, EXTENDED RELEASE;ORAL - 2MG
        • TABLET, EXTENDED RELEASE;ORAL - 3MG
        • TABLET, ORALLY DISINTEGRATING;ORAL - 0.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
        • TABLET, ORALLY DISINTEGRATING;ORAL - 0.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
        • TABLET, ORALLY DISINTEGRATING;ORAL - 1MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
        • TABLET, ORALLY DISINTEGRATING;ORAL - 2MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
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