BONTRIL - 12634-782-78 - (PHENDIMETRAZINE TARTRATE)

Alphabetical Index


Drug Information of BONTRIL

Product NDC: 12634-782
Proprietary Name: BONTRIL
Non Proprietary Name: PHENDIMETRAZINE TARTRATE
Active Ingredient(s): 105    mg/1 & nbsp;   PHENDIMETRAZINE TARTRATE
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of BONTRIL

Product NDC: 12634-782
Labeler Name: Apotheca, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA088021
Marketing Category: ANDA
Start Marketing Date: 20100408

Package Information of BONTRIL

Package NDC: 12634-782-78
Package Description: 28 CAPSULE in 1 BOTTLE (12634-782-78)

NDC Information of BONTRIL

NDC Code 12634-782-78
Proprietary Name BONTRIL
Package Description 28 CAPSULE in 1 BOTTLE (12634-782-78)
Product NDC 12634-782
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PHENDIMETRAZINE TARTRATE
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20100408
Marketing Category Name ANDA
Labeler Name Apotheca, Inc.
Substance Name PHENDIMETRAZINE TARTRATE
Strength Number 105
Strength Unit mg/1
Pharmaceutical Classes Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC]

Complete Information of BONTRIL


General Information