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Recede - 50991-399-01 - (benzphetamine hydrochloride)
Drug Information of Recede
| Product NDC: | 50991-399 |
| Proprietary Name: | Recede |
| Non Proprietary Name: | benzphetamine hydrochloride |
| Active Ingredient(s): | 25 mg/1 & nbsp; benzphetamine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Recede
| Product NDC: | 50991-399 |
| Labeler Name: | Poly Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090473 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120201 |
Package Information of Recede
| Package NDC: | 50991-399-01 |
| Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (50991-399-01) |
NDC Information of Recede
| NDC Code | 50991-399-01 |
| Proprietary Name | Recede |
| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (50991-399-01) |
| Product NDC | 50991-399 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | benzphetamine hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120201 |
| Marketing Category Name | ANDA |
| Labeler Name | Poly Pharmaceuticals, Inc. |
| Substance Name | BENZPHETAMINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC] |
