Search by Drug Name or NDC
NDC 43063-0541-98 BENZPHETAMINE HYDROCHLORIDE 50 mg/1 Details
BENZPHETAMINE HYDROCHLORIDE 50 mg/1
BENZPHETAMINE HYDROCHLORIDE is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by PD-Rx Pharmaceuticals, Inc.. The primary component is BENZPHETAMINE HYDROCHLORIDE.
Product Information
| NDC | 43063-0541 |
|---|---|
| Product ID | 43063-541_f8c334d7-1b52-94a7-e053-6294a90a2aed |
| 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 |
| Route | ORAL |
| Active Ingredient Strength | 50 |
| Active Ingredient Units | mg/1 |
| Substance Name | BENZPHETAMINE HYDROCHLORIDE |
| Labeler Name | PD-Rx Pharmaceuticals, Inc. |
| Pharmaceutical Class | Appetite Suppression [PE], Increased Sympathetic Activity [PE], Sympathomimetic Amine Anorectic [EPC] |
| DEA Schedule | CIII |
| Marketing Category | ANDA |
| Application Number | ANDA090968 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 43063-0541-98 (43063054198)
| NDC Package Code | 43063-541-98 |
|---|---|
| Billing NDC | 43063054198 |
| Package | 120 TABLET in 1 BOTTLE, PLASTIC (43063-541-98) |
| Marketing Start Date | 2010-07-21 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |