Active ingredient
Tranylcypromine
6 finished FDA listings contain Tranylcypromine as their only active ingredient.
FDA NDC Directory
- Ingredient names as written by FDA
- TRANYLCYPROMINE SULFATE
- Dosage forms
- Tablet, Tablet, Film Coated
- Routes
- Oral
- Manufacturers / labelers
- 6
- Strengths listed
- 10 mg/1
- Brand names in FDA listings
- Parnate
RxNorm (National Library of Medicine)
Ingredient concept RxCUI 10734
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 |
|---|---|---|---|
| NDA 012342 | ADVANZ PHARMA | 1961-02-21 | 2 |
| ANDA 040640 | STRIDES PHARMA INTL | 2006-06-29 | 1 |
| ANDA 206856 | NOVITIUM PHARMA | 2018-04-17 | 1 |
| ANDA 213503 | CROSSMEDIKA SA | 2022-06-27 | 2 |
Official labeling on DailyMed
- TRANYLCYPROMINE TABLET [REMEDYREPACK INC.] · version 1 · 2026-07-24
- TRANYLCYPROMINE SULFATE TABLET, FILM COATED [ACTAVIS PHARMA, INC.] · version 8 · 2025-07-28
- PARNATE (TRANYLCYPROMINE SULFATE) TABLET, FILM COATED [ADVANZ PHARMA (US) CORP.] · version 11 · 2025-07-07
- TRANYLCYPROMINE TABLET [SOLCO HEALTHCARE US, LLC] · version 3 · 2024-12-25
- TRANYLCYPROMINE SULFATE TABLET, FILM COATED [STRIDES PHARMA SCIENCE LIMITED] · version 3 · 2023-05-29
- TRANYLCYPROMINE TABLET [NOVITIUM PHARMA LLC] · version 1 · 2021-06-22
Sources: FDA NDC Directory (2026-09-29), RxNorm, Drugs@FDA, DailyMed. Each source’s facts are shown separately as published.