ZOFRAN - 0173-0446-02 - (ondansetron hydrochloride)

Alphabetical Index


Drug Information of ZOFRAN

Product NDC: 0173-0446
Proprietary Name: ZOFRAN
Non Proprietary Name: ondansetron hydrochloride
Active Ingredient(s): 4    mg/1 & nbsp;   ondansetron hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of ZOFRAN

Product NDC: 0173-0446
Labeler Name: GlaxoSmithKline LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020103
Marketing Category: NDA
Start Marketing Date: 19930211

Package Information of ZOFRAN

Package NDC: 0173-0446-02
Package Description: 100 TABLET, FILM COATED in 1 DOSE PACK (0173-0446-02)

NDC Information of ZOFRAN

NDC Code 0173-0446-02
Proprietary Name ZOFRAN
Package Description 100 TABLET, FILM COATED in 1 DOSE PACK (0173-0446-02)
Product NDC 0173-0446
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ondansetron hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19930211
Marketing Category Name NDA
Labeler Name GlaxoSmithKline LLC
Substance Name ONDANSETRON HYDROCHLORIDE
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]

Complete Information of ZOFRAN


General Information