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GRANISETRON HYDROCHLORIDE - 64720-198-97 - (GRANISETRON HYDROCHLORIDE)

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Drug Information of GRANISETRON HYDROCHLORIDE

Product NDC: 64720-198
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, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of GRANISETRON HYDROCHLORIDE

Product NDC: 64720-198
Labeler Name: COREPHARMA LLC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078260
Marketing Category: ANDA
Start Marketing Date: 20071231

Package Information of GRANISETRON HYDROCHLORIDE

Package NDC: 64720-198-97
Package Description: 20 TABLET, FILM COATED in 1 BLISTER PACK (64720-198-97)

NDC Information of GRANISETRON HYDROCHLORIDE

NDC Code 64720-198-97
Proprietary Name GRANISETRON HYDROCHLORIDE
Package Description 20 TABLET, FILM COATED in 1 BLISTER PACK (64720-198-97)
Product NDC 64720-198
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name GRANISETRON HYDROCHLORIDE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20071231
Marketing Category Name ANDA
Labeler Name COREPHARMA LLC.
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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