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Granisetron Hydrochloride - 0054-0143-08 - (Granisetron Hydrochloride)

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Drug Information of Granisetron Hydrochloride

Product NDC: 0054-0143
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: 0054-0143
Labeler Name: Roxane Laboratories, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077842
Marketing Category: ANDA
Start Marketing Date: 20080516

Package Information of Granisetron Hydrochloride

Package NDC: 0054-0143-08
Package Description: 10 BLISTER PACK in 1 CARTON (0054-0143-08) > 2 TABLET in 1 BLISTER PACK

NDC Information of Granisetron Hydrochloride

NDC Code 0054-0143-08
Proprietary Name Granisetron Hydrochloride
Package Description 10 BLISTER PACK in 1 CARTON (0054-0143-08) > 2 TABLET in 1 BLISTER PACK
Product NDC 0054-0143
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Granisetron Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080516
Marketing Category Name ANDA
Labeler Name Roxane Laboratories, 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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