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