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NDC 17224-0672-30 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 Calvin Scott & Co., Inc.. The primary component is BENZPHETAMINE HYDROCHLORIDE.
Product Information
| NDC | 17224-0672 |
|---|---|
| Product ID | 17224-672_f5ee265f-9765-de77-e053-2a95a90ac76f |
| 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 | Calvin Scott & Co., 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 17224-0672-30 (17224067230)
| NDC Package Code | 17224-672-30 |
|---|---|
| Billing NDC | 17224067230 |
| Package | 30 TABLET in 1 BOTTLE, PLASTIC (17224-672-30) |
| Marketing Start Date | 2010-01-01 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |