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GRANISETRON HYDROCHLORIDE - 55648-661-01 - (GRANISETRON HYDROCHLORIDE)

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Drug Information of GRANISETRON HYDROCHLORIDE

Product NDC: 55648-661
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: 55648-661
Labeler Name: WOCKHARDT LIMITED
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078564
Marketing Category: ANDA
Start Marketing Date: 20080630

Package Information of GRANISETRON HYDROCHLORIDE

Package NDC: 55648-661-01
Package Description: 5 CARTON in 1 CARTON (55648-661-01) > 1 VIAL, SINGLE-USE in 1 CARTON (55648-661-03) > 1 mL in 1 VIAL, SINGLE-USE

NDC Information of GRANISETRON HYDROCHLORIDE

NDC Code 55648-661-01
Proprietary Name GRANISETRON HYDROCHLORIDE
Package Description 5 CARTON in 1 CARTON (55648-661-01) > 1 VIAL, SINGLE-USE in 1 CARTON (55648-661-03) > 1 mL in 1 VIAL, SINGLE-USE
Product NDC 55648-661
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name GRANISETRON HYDROCHLORIDE
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20080630
Marketing Category Name ANDA
Labeler Name WOCKHARDT LIMITED
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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