FDA NDC Directory · JSON-LD · Markdown
NDC 58151-126 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE
| Generic name | VENLAFAXINE HYDROCHLORIDE |
|---|---|
| Labeler / Manufacturer | Viatris Specialty LLC |
| Marketing category | New Drug Application (innovator) · App NDA020699 |
| Dosage form / route | CAPSULE, EXTENDED RELEASE · ORAL |
| Active ingredients | VENLAFAXINE HYDROCHLORIDE (75 mg/1) |
| Marketing started | 20241030 |
| Package count | 2 |
Source: openFDA. Public-domain (CC0).