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NDC 71335-0451-01 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 Bryant Ranch Prepack. The primary component is BENZPHETAMINE HYDROCHLORIDE.
Product Information
| NDC | 71335-0451 |
|---|---|
| Product ID | 71335-0451_e5454571-1da1-4eaa-bb5c-a478ee3aa663 |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| 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 | Bryant Ranch Prepack |
| 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 71335-0451-01 (71335045101)
| NDC Package Code | 71335-0451-1 |
|---|---|
| Billing NDC | 71335045101 |
| Package | 30 TABLET in 1 BOTTLE (71335-0451-1) |
| Marketing Start Date | 2018-08-17 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |