Anzemet - 0088-1203-29 - (dolasetron mesylate)

Alphabetical Index


Drug Information of Anzemet

Product NDC: 0088-1203
Proprietary Name: Anzemet
Non Proprietary Name: dolasetron mesylate
Active Ingredient(s): 100    mg/1 & nbsp;   dolasetron mesylate
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Anzemet

Product NDC: 0088-1203
Labeler Name: sanofi-aventis U.S. LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020623
Marketing Category: NDA
Start Marketing Date: 19970911

Package Information of Anzemet

Package NDC: 0088-1203-29
Package Description: 5 TABLET, FILM COATED in 1 BLISTER PACK (0088-1203-29)

NDC Information of Anzemet

NDC Code 0088-1203-29
Proprietary Name Anzemet
Package Description 5 TABLET, FILM COATED in 1 BLISTER PACK (0088-1203-29)
Product NDC 0088-1203
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name dolasetron mesylate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19970911
Marketing Category Name NDA
Labeler Name sanofi-aventis U.S. LLC
Substance Name DOLASETRON MESYLATE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]

Complete Information of Anzemet


General Information