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Regimex
Regimex - 66992-399-10 - (benzphetamine hydrochloride)
Drug Information of Regimex
| Product NDC: | 66992-399 |
| Proprietary Name: | Regimex |
| 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 Regimex
| Product NDC: | 66992-399 |
| Labeler Name: | Wraser Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090473 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130201 |
Package Information of Regimex
| Package NDC: | 66992-399-10 |
| Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (66992-399-10) |
NDC Information of Regimex
| NDC Code | 66992-399-10 |
| Proprietary Name | Regimex |
| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (66992-399-10) |
| Product NDC | 66992-399 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | benzphetamine hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130201 |
| Marketing Category Name | ANDA |
| Labeler Name | Wraser Pharmaceuticals |
| Substance Name | BENZPHETAMINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC] |
