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