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