Benzphetamine Hydrochloride
- Product NDC
- 50090-5837
- 11-digit product format
- 500905837
- Labeler code
- 50090
- Product ID
- 50090-5837_06aa2799-9910-4cbd-b44f-50755a51536e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benzphetamine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA090346
- Marketing category
- ANDA
- Marketing start
- 2015-12-16
- 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
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5837-1 | 50090583701 | 60 TABLET, FILM COATED in 1 BOTTLE (50090-5837-1) | 2021-10-29 | 0000-00-00 | No | No | Current |
| 50090-5837-2 | 50090583702 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-5837-2) | 2021-11-02 | 0000-00-00 | No | No | Current |