Trental - 0039-0078-10 - (pentoxifylline)

Alphabetical Index


Drug Information of Trental

Product NDC: 0039-0078
Proprietary Name: Trental
Non Proprietary Name: pentoxifylline
Active Ingredient(s): 400    mg/1 & nbsp;   pentoxifylline
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Trental

Product NDC: 0039-0078
Labeler Name: Sanofi-Aventis U.S. LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018631
Marketing Category: NDA
Start Marketing Date: 19840830

Package Information of Trental

Package NDC: 0039-0078-10
Package Description: 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0039-0078-10)

NDC Information of Trental

NDC Code 0039-0078-10
Proprietary Name Trental
Package Description 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0039-0078-10)
Product NDC 0039-0078
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name pentoxifylline
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19840830
Marketing Category Name NDA
Labeler Name Sanofi-Aventis U.S. LLC
Substance Name PENTOXIFYLLINE
Strength Number 400
Strength Unit mg/1
Pharmaceutical Classes Blood Viscosity Reducer [EPC],Hematologic Activity Alteration [PE]

Complete Information of Trental


General Information