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Phendimetrazine Tartrate
Phendimetrazine Tartrate - 52959-282-35 - (Phendimetrazine Tartrate)
Drug Information of Phendimetrazine Tartrate
| Product NDC: | 52959-282 |
| Proprietary Name: | Phendimetrazine Tartrate |
| 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 Phendimetrazine Tartrate
| Product NDC: | 52959-282 |
| Labeler Name: | H.J. Harkins Company, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091042 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100915 |
Package Information of Phendimetrazine Tartrate
| Package NDC: | 52959-282-35 |
| Package Description: | 35 TABLET in 1 BOTTLE (52959-282-35) |
NDC Information of Phendimetrazine Tartrate
| NDC Code | 52959-282-35 |
| Proprietary Name | Phendimetrazine Tartrate |
| Package Description | 35 TABLET in 1 BOTTLE (52959-282-35) |
| Product NDC | 52959-282 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Phendimetrazine Tartrate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100915 |
| Marketing Category Name | ANDA |
| Labeler Name | H.J. Harkins Company, Inc. |
| Substance Name | PHENDIMETRAZINE TARTRATE |
| Strength Number | 35 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC] |
