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Bontril PDM - 0187-0497-02 - (Phendimetrazine Tartrate)

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Drug Information of Bontril PDM

Product NDC: 0187-0497
Proprietary Name: Bontril PDM
Non Proprietary Name: Phendimetrazine Tartrate
Active Ingredient(s): 35    mg/1 & nbsp;   Phendimetrazine Tartrate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Bontril PDM

Product NDC: 0187-0497
Labeler Name: Valeant Pharmaceuticals International
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA085272
Marketing Category: ANDA
Start Marketing Date: 19761222

Package Information of Bontril PDM

Package NDC: 0187-0497-02
Package Description: 1000 TABLET in 1 BOTTLE, PLASTIC (0187-0497-02)

NDC Information of Bontril PDM

NDC Code 0187-0497-02
Proprietary Name Bontril PDM
Package Description 1000 TABLET in 1 BOTTLE, PLASTIC (0187-0497-02)
Product NDC 0187-0497
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Phendimetrazine Tartrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19761222
Marketing Category Name ANDA
Labeler Name Valeant Pharmaceuticals International
Substance Name PHENDIMETRAZINE TARTRATE
Strength Number 35
Strength Unit mg/1
Pharmaceutical Classes Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC]

Complete Information of Bontril PDM


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