Active ingredient
Benzphetamine
6 finished FDA listings contain Benzphetamine as their only active ingredient.
FDA NDC Directory
- Ingredient names as written by FDA
- BENZPHETAMINE, BENZPHETAMINE HYDROCHLORIDE
- Dosage forms
- Tablet, Tablet, Film Coated
- Routes
- Oral
- Manufacturers / labelers
- 6
- Strengths listed
- 50 mg/1
RxNorm (National Library of Medicine)
Ingredient concept RxCUI 1422
Drugs@FDA applications
Linked only where the FDA listing’s application number matches Drugs@FDA exactly. A listing in the NDC Directory does not by itself mean FDA approval.
| Application | Sponsor | Original approval | Listings |
|---|---|---|---|
| ANDA 090968 | KVK TECH | 2010-07-20 | 4 |
| ANDA 202061 | AVET LIFESCIENCES | 2012-01-27 | 1 |
| ANDA 090346 | EPIC PHARMA LLC | 2015-12-15 | 1 |
Official labeling on DailyMed
- BENZPHETAMINE HYDROCHLORIDE TABLET [KVK-TECH, INC] · version 10 · 2026-08-03
- BENZPHETAMINE HYDROCHLORIDE TABLET, FILM COATED [HERITAGE PHARMACEUTICALS INC. D/B/A AVET PHARMACEUTICALS INC.] · version 1 · 2026-06-22
- BENZPHETAMINE HYDROCHLORIDE TABLET [BRYANT RANCH PREPACK] · version 10 · 2024-06-03
- BENZPHETAMINE HYDROCHLORIDE TABLET, FILM COATED [EPIC PHARMA, LLC] · version 8 · 2023-12-28
- BENZPHETAMINE HYDROCHLORIDE TABLET [CALVIN SCOTT & CO., INC.] · version 2 · 2023-03-03
Sources: FDA NDC Directory (2026-09-29), RxNorm, Drugs@FDA, DailyMed. Each source’s facts are shown separately as published.