FDA NDC Directory · JSON-LD · Markdown
NDC 23155-249 · HUMAN PRESCRIPTION DRUG · TABLET
| Labeler / Manufacturer | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA078554 |
| Dosage form / route | TABLET · ORAL |
| Active ingredients | VENLAFAXINE HYDROCHLORIDE (75 mg/1) |
| Marketing started | 20210719 |
| Package count | 2 |
Source: openFDA. Public-domain (CC0).