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phendimetrazine tartrate
phendimetrazine tartrate - 0463-8500-10 - (phendimetrazine tartrate)
Drug Information of phendimetrazine tartrate
| Product NDC: | 0463-8500 |
| 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: | 0463-8500 |
| Labeler Name: | C.O. Truxton, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA089452 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20010726 |
Package Information of phendimetrazine tartrate
| Package NDC: | 0463-8500-10 |
| Package Description: | 1000 TABLET in 1 BOTTLE, PLASTIC (0463-8500-10) |
NDC Information of phendimetrazine tartrate
| NDC Code | 0463-8500-10 |
| Proprietary Name | phendimetrazine tartrate |
| Package Description | 1000 TABLET in 1 BOTTLE, PLASTIC (0463-8500-10) |
| Product NDC | 0463-8500 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | phendimetrazine tartrate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20010726 |
| Marketing Category Name | ANDA |
| Labeler Name | C.O. Truxton, 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] |
