NDC 23155-952 – Benzphetamine Hydrochloride
Benzphetamine Hydrochloride 50 mg/1 · Tablet, Film Coated · Oral
Product NDC23155-952
Product details
- Brand name
- Benzphetamine Hydrochloride
- Generic name
- Benzphetamine Hydrochloride
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA202061
- Marketed since
- June 19, 2026
- Listing expires
- December 31, 2027
- Pharmacologic class
- Sympathomimetic Amine Anorectic
Active ingredients
- Benzphetamine Hydrochloride 50 mg/1
Uses, dosage, side effects and warnings for Benzphetamine Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 23155-952-01 | 100 TABLET, FILM COATED in 1 BOTTLE (23155-952-01) | Jun 19, 2026 |
| 23155-952-03 | 30 TABLET, FILM COATED in 1 BOTTLE (23155-952-03) | Jun 19, 2026 |
| 23155-952-05 | 500 TABLET, FILM COATED in 1 BOTTLE (23155-952-05) | Jun 19, 2026 |
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