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granisetron hydrochloride - 25021-779-01 - (granisetron hydrochloride)

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Drug Information of granisetron hydrochloride

Product NDC: 25021-779
Proprietary Name: granisetron hydrochloride
Non Proprietary Name: granisetron hydrochloride
Active Ingredient(s): 1    mg/mL & nbsp;   granisetron hydrochloride
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of granisetron hydrochloride

Product NDC: 25021-779
Labeler Name: Sagent Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091136
Marketing Category: ANDA
Start Marketing Date: 20101201

Package Information of granisetron hydrochloride

Package NDC: 25021-779-01
Package Description: 1 VIAL in 1 CARTON (25021-779-01) > 1 mL in 1 VIAL

NDC Information of granisetron hydrochloride

NDC Code 25021-779-01
Proprietary Name granisetron hydrochloride
Package Description 1 VIAL in 1 CARTON (25021-779-01) > 1 mL in 1 VIAL
Product NDC 25021-779
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name granisetron hydrochloride
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20101201
Marketing Category Name ANDA
Labeler Name Sagent Pharmaceuticals
Substance Name GRANISETRON HYDROCHLORIDE
Strength Number 1
Strength Unit mg/mL
Pharmaceutical Classes Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]

Complete Information of granisetron hydrochloride


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