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
FDA-Initiated Inactive NDC Indexing#