Benzphetamine Hydrochloride
- Product NDC
- 63629-4139
- 11-digit product format
- 636294139
- Labeler code
- 63629
- Product ID
- 63629-4139_c09c2424-b088-4211-bd2e-67a10602fd92
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benzphetamine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- bryant ranch prepack
- Application
- ANDA040845
- Marketing category
- ANDA
- Marketing start
- 2010-02-01
- Marketing end
- 0000-00-00
- Substance
- BENZPHETAMINE HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC]
- DEA schedule
- CIII
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 63629-4139 | D | Discontinued by firm | 2026-07-31 | ||
| excluded package | package | 63629-4139 | 63629-4139-1 | D | Discontinued by firm | 2026-07-31 | |
| excluded package | package | 63629-4139 | 63629-4139-2 | D | Discontinued by firm | 2026-07-31 | |
| excluded package | package | 63629-4139 | 63629-4139-3 | D | Discontinued by firm | 2026-07-31 | |
| excluded package | package | 63629-4139 | 63629-4139-4 | D | Discontinued by firm | 2026-07-31 | |
| excluded package | package | 63629-4139 | 63629-4139-5 | D | Discontinued by firm | 2026-07-31 | |
| excluded package | package | 63629-4139 | 63629-4139-6 | D | Discontinued by firm | 2026-07-31 | |
| excluded package | package | 63629-4139 | 63629-4139-7 | D | Discontinued by firm | 2026-07-31 | |
| excluded package | package | 63629-4139 | 63629-4139-8 | D | Discontinued by firm | 2026-07-31 | |
| excluded package | package | 63629-4139 | 63629-4139-9 | D | Discontinued by firm | 2026-07-31 |
Orange Book products#
| Application-product | Trade name | Ingredient | Strength | Dosage form / route | TE codes | RLD / RS | Approval date |
|---|---|---|---|---|---|---|---|
| A040845-001 | BENZPHETAMINE HYDROCHLORIDE | BENZPHETAMINE HYDROCHLORIDE | 50MG | TABLET / ORAL | 2008-11-18 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 63629-4139-1 | EA - Each | 63629-4139 | affac325-e7ee-4156-a89d-84461a663892 | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| BENZPHETAMINE HYDROCHLORIDE | ACTIVE INGREDIENT | 43DWT87QT7 | BENZPHETAMINE HYDROCHLORIDE TABLET [BRYANT RANCH PREPACK] | 2 | |
| BENZPHETAMINE | ACTIVE MOIETY | 0M3S43XK27 | BENZPHETAMINE HYDROCHLORIDE TABLET [BRYANT RANCH PREPACK] | 2 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | BENZPHETAMINE HYDROCHLORIDE TABLET [BRYANT RANCH PREPACK] | 2 | |
| LACTOSE MONOHYDRATE | INACTIVE INGREDIENT | EWQ57Q8I5X | BENZPHETAMINE HYDROCHLORIDE TABLET [BRYANT RANCH PREPACK] | 2 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | BENZPHETAMINE HYDROCHLORIDE TABLET [BRYANT RANCH PREPACK] | 2 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | BENZPHETAMINE HYDROCHLORIDE TABLET [BRYANT RANCH PREPACK] | 2 |