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Granisetron Hydrochloride - 17478-547-01 - (Granisetron Hydrochloride)

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Drug Information of Granisetron Hydrochloride

Product NDC: 17478-547
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: 17478-547
Labeler Name: Akorn Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079119
Marketing Category: ANDA
Start Marketing Date: 20091001

Package Information of Granisetron Hydrochloride

Package NDC: 17478-547-01
Package Description: 10 VIAL, GLASS in 1 CARTON (17478-547-01) > 1 mL in 1 VIAL, GLASS

NDC Information of Granisetron Hydrochloride

NDC Code 17478-547-01
Proprietary Name Granisetron Hydrochloride
Package Description 10 VIAL, GLASS in 1 CARTON (17478-547-01) > 1 mL in 1 VIAL, GLASS
Product NDC 17478-547
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Granisetron Hydrochloride
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20091001
Marketing Category Name ANDA
Labeler Name Akorn Inc.
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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