Bontril - 0187-0498-02 - (Phendimetrazine Tartrate)

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Drug Information of Bontril

Product NDC: 0187-0498
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: 0187-0498
Labeler Name: Valeant Pharmaceuticals International
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA088021
Marketing Category: ANDA
Start Marketing Date: 19820921

Package Information of Bontril

Package NDC: 0187-0498-02
Package Description: 1000 CAPSULE in 1 BOTTLE (0187-0498-02)

NDC Information of Bontril

NDC Code 0187-0498-02
Proprietary Name Bontril
Package Description 1000 CAPSULE in 1 BOTTLE (0187-0498-02)
Product NDC 0187-0498
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Phendimetrazine Tartrate
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19820921
Marketing Category Name ANDA
Labeler Name Valeant Pharmaceuticals International
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