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NDC 50090-5837-00 Benzphetamine Hydrochloride 50 mg/1 Details
Benzphetamine Hydrochloride 50 mg/1
Benzphetamine Hydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by A-S Medication Solutions. The primary component is BENZPHETAMINE HYDROCHLORIDE.
Product Information
| NDC | 50090-5837 |
|---|---|
| Product ID | 50090-5837_b01fbcb4-85b5-4a89-8a38-992bbec68ea5 |
| Associated GPIs | 61200010100310 |
| GCN Sequence Number | 005021 |
| GCN Sequence Number Description | benzphetamine HCl TABLET 50 MG ORAL |
| HIC3 | J8A |
| HIC3 Description | ANTI-OBESITY - ANOREXIC AGENTS |
| GCN | 19981 |
| HICL Sequence Number | 002070 |
| HICL Sequence Number Description | BENZPHETAMINE HCL |
| Brand/Generic | Generic |
| Proprietary Name | Benzphetamine Hydrochloride |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Benzphetamine Hydrochloride |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET, FILM COATED |
| Route | ORAL |
| Active Ingredient Strength | 50 |
| Active Ingredient Units | mg/1 |
| Substance Name | BENZPHETAMINE HYDROCHLORIDE |
| Labeler Name | A-S Medication Solutions |
| Pharmaceutical Class | Appetite Suppression [PE], Increased Sympathetic Activity [PE], Sympathomimetic Amine Anorectic [EPC] |
| DEA Schedule | CIII |
| Marketing Category | ANDA |
| Application Number | ANDA090346 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 50090-5837-00 (50090583700)
| NDC Package Code | 50090-5837-0 |
|---|---|
| Billing NDC | 50090583700 |
| Package | 30 TABLET, FILM COATED in 1 BOTTLE (50090-5837-0) |
| Marketing Start Date | 2021-10-29 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |