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Granisetron Hydrochloride - 51991-735-32 - (Granisetron Hydrochloride)

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Drug Information of Granisetron Hydrochloride

Product NDC: 51991-735
Proprietary Name: Granisetron Hydrochloride
Non Proprietary Name: Granisetron Hydrochloride
Active Ingredient(s): 1    mg/1 & nbsp;   Granisetron Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Granisetron Hydrochloride

Product NDC: 51991-735
Labeler Name: Breckenridge Pharmaceutical, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078969
Marketing Category: ANDA
Start Marketing Date: 20090622

Package Information of Granisetron Hydrochloride

Package NDC: 51991-735-32
Package Description: 1 BLISTER PACK in 1 CARTON (51991-735-32) > 2 TABLET in 1 BLISTER PACK

NDC Information of Granisetron Hydrochloride

NDC Code 51991-735-32
Proprietary Name Granisetron Hydrochloride
Package Description 1 BLISTER PACK in 1 CARTON (51991-735-32) > 2 TABLET in 1 BLISTER PACK
Product NDC 51991-735
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Granisetron Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090622
Marketing Category Name ANDA
Labeler Name Breckenridge Pharmaceutical, Inc.
Substance Name GRANISETRON HYDROCHLORIDE
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]

Complete Information of Granisetron Hydrochloride


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