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DIDREX
DIDREX - 0009-0024-02 - (benzphetamine hydrochloride)
Drug Information of DIDREX
| Product NDC: | 0009-0024 |
| Proprietary Name: | DIDREX |
| Non Proprietary Name: | benzphetamine hydrochloride |
| Active Ingredient(s): | 50 mg/1 & nbsp; benzphetamine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DIDREX
| Product NDC: | 0009-0024 |
| Labeler Name: | Pharmacia and Upjohn Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA012427 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19601026 |
Package Information of DIDREX
| Package NDC: | 0009-0024-02 |
| Package Description: | 500 TABLET in 1 BOTTLE (0009-0024-02) |
NDC Information of DIDREX
| NDC Code | 0009-0024-02 |
| Proprietary Name | DIDREX |
| Package Description | 500 TABLET in 1 BOTTLE (0009-0024-02) |
| Product NDC | 0009-0024 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | benzphetamine hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19601026 |
| Marketing Category Name | NDA |
| Labeler Name | Pharmacia and Upjohn Company |
| Substance Name | BENZPHETAMINE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC] |
