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List of Suppliers' Fillers Diluents Binders Excipients Application used in Gemcitabine Hydrochloride on PharmaCompass.com

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LM Application #LearnMore
Ingredient(s): Mannitol
Dosage Form: Capsule, Suspension, Syrup, Tablet
Route of Administration (Grade): Oral
Pharmacopoeia Reference: IP/BP/EP/USP-NF
Technical Specifications: NA

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LM Application #LearnMore
Ingredient(s): Mannitol
Route of Administration (Grade): Not Available
Pharmacopoeia Reference: CP/BP/ EP/ USP/IP
Technical Specifications: Pharma Grade/ Medicine Grade/Injectable Grade
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LM Application #LearnMore
Ingredient(s): Mannitol
Dosage Form: Tablet
Route of Administration (Grade): Oral
Pharmacopoeia Reference: USP/NF, Ph. Eur.
Technical Specifications: NA
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LM Application #LearnMore
Ingredient(s): Mannitol
Dosage Form: Capsule, Tablet
Route of Administration (Grade): Oral
Pharmacopoeia Reference: Not Available
Technical Specifications: Not Available
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LM Application #LearnMore
Ingredient(s): Mannitol
Dosage Form: Tablet
Route of Administration (Grade): Not Available
Pharmacopoeia Reference: USP/NF, EP, JP, ChP
Technical Specifications: Not Available
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LM Application #LearnMore
Ingredient(s): Mannitol, Starch
Route of Administration (Grade): Not Available
Pharmacopoeia Reference: Not Available
Technical Specifications: Not Available
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LM Application #LearnMore
Ingredient(s): Mannitol
Dosage Form: Capsule, Tablet
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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LM Application #LearnMore
Ingredient(s): Crospovidone
Route of Administration (Grade): Oral
Pharmacopoeia Reference: Conforms to Japanese Pharmaceutical Excipients. All components meet USP-NF, JP, EP. US DMF Type IV filed.
Technical Specifications: Not Available
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LM Application #LearnMore
Ingredient(s): Mannitol
Route of Administration (Grade): Not Available
Pharmacopoeia Reference: EP/USP/JP
Technical Specifications: Not Available
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  • INJECTABLE;INJECTION - EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • INJECTABLE;INJECTION - EQ 200MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • SOLUTION;INTRAVENOUS - EQ 1200MG BASE/120ML (EQ 10MG BASE/ML)
  • SOLUTION;INTRAVENOUS - EQ 1300MG BASE/130ML (EQ 10MG BASE/ML)
  • SOLUTION;INTRAVENOUS - EQ 1400MG BASE/140ML (EQ 10MG BASE/ML)
  • SOLUTION;INTRAVENOUS - EQ 1500MG BASE/150ML (EQ 10MG BASE/ML)
  • SOLUTION;INTRAVENOUS - EQ 1600MG BASE/160ML (EQ 10MG BASE/ML)
  • SOLUTION;INTRAVENOUS - EQ 1700MG BASE/170ML (EQ 10MG BASE/ML)
  • SOLUTION;INTRAVENOUS - EQ 1800MG BASE/180ML (EQ 10MG BASE/ML)
  • SOLUTION;INTRAVENOUS - EQ 1900MG BASE/190ML (EQ 10MG BASE/ML)
  • SOLUTION;INTRAVENOUS - EQ 2000MG BASE/200ML (EQ 10MG BASE/ML)
  • SOLUTION;INTRAVENOUS - EQ 2200MG BASE/220ML (EQ 10MG BASE/ML)
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