Benzphetamine Hydrochloride 23155-0952
Product NDC
23155-0952- Manufacturer
- Heritage Pharmaceuticals Inc. D/b/a Avet Pharmaceuticals Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIII
- Marketing Start
- June 19, 2026
- Listing Expires
- December 31, 2027
- Application
- ANDA202061
Active Ingredients
| Ingredient | Strength |
|---|---|
| Benzphetamine Hydrochloride | 50 mg/1 |
Drug Class
Appetite Suppression [PE]Increased Sympathetic Activity [PE]Sympathomimetic Amine Anorectic [EPC]
Packaging Options(3)
100 TABLET, FILM COATED in 1 BOTTLE (23155-952-01)
30 TABLET, FILM COATED in 1 BOTTLE (23155-952-03)
500 TABLET, FILM COATED in 1 BOTTLE (23155-952-05)