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PHENDIMETRAZINE TARTRATE
PHENDIMETRAZINE TARTRATE - 45963-327-11 - (Phendimetrazine Tartrate)
Drug Information of PHENDIMETRAZINE TARTRATE
| Product NDC: | 45963-327 |
| 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: | 45963-327 |
| Labeler Name: | Actavis, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040762 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20121120 |
Package Information of PHENDIMETRAZINE TARTRATE
| Package NDC: | 45963-327-11 |
| Package Description: | 100 TABLET in 1 BOTTLE (45963-327-11) |
NDC Information of PHENDIMETRAZINE TARTRATE
| NDC Code | 45963-327-11 |
| Proprietary Name | PHENDIMETRAZINE TARTRATE |
| Package Description | 100 TABLET in 1 BOTTLE (45963-327-11) |
| Product NDC | 45963-327 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Phendimetrazine Tartrate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20121120 |
| Marketing Category Name | ANDA |
| Labeler Name | Actavis, 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] |
