ZOFRAN - 0173-0442-00 - (ondansetron hydrochloride)

Alphabetical Index


Drug Information of ZOFRAN

Product NDC: 0173-0442
Proprietary Name: ZOFRAN
Non Proprietary Name: ondansetron hydrochloride
Active Ingredient(s): 2    mg/mL & nbsp;   ondansetron hydrochloride
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of ZOFRAN

Product NDC: 0173-0442
Labeler Name: GlaxoSmithKline LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020007
Marketing Category: NDA
Start Marketing Date: 19910204

Package Information of ZOFRAN

Package NDC: 0173-0442-00
Package Description: 20 mL in 1 VIAL (0173-0442-00)

NDC Information of ZOFRAN

NDC Code 0173-0442-00
Proprietary Name ZOFRAN
Package Description 20 mL in 1 VIAL (0173-0442-00)
Product NDC 0173-0442
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ondansetron hydrochloride
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 19910204
Marketing Category Name NDA
Labeler Name GlaxoSmithKline LLC
Substance Name ONDANSETRON HYDROCHLORIDE
Strength Number 2
Strength Unit mg/mL
Pharmaceutical Classes Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]

Complete Information of ZOFRAN


General Information