Anzemet - 0088-1208-06 - (dolasetron mesylate)

Alphabetical Index


Drug Information of Anzemet

Product NDC: 0088-1208
Proprietary Name: Anzemet
Non Proprietary Name: dolasetron mesylate
Active Ingredient(s): 12.5    mg/.625mL & nbsp;   dolasetron mesylate
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Anzemet

Product NDC: 0088-1208
Labeler Name: sanofi-aventis U.S. LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020624
Marketing Category: NDA
Start Marketing Date: 19970911

Package Information of Anzemet

Package NDC: 0088-1208-06
Package Description: 6 VIAL, SINGLE-USE in 1 BOX (0088-1208-06) > .625 mL in 1 VIAL, SINGLE-USE

NDC Information of Anzemet

NDC Code 0088-1208-06
Proprietary Name Anzemet
Package Description 6 VIAL, SINGLE-USE in 1 BOX (0088-1208-06) > .625 mL in 1 VIAL, SINGLE-USE
Product NDC 0088-1208
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name dolasetron mesylate
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 19970911
Marketing Category Name NDA
Labeler Name sanofi-aventis U.S. LLC
Substance Name DOLASETRON MESYLATE
Strength Number 12.5
Strength Unit mg/.625mL
Pharmaceutical Classes Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]

Complete Information of Anzemet


General Information