Venlafaxine
- Product NDC
- 68071-2990
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA077653
- Marketing category
- ANDA
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 68071-2990-9 | 90 TABLET in 1 BOTTLE (68071-2990-9) | 2023-04-24 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Venlafaxine Tablets, USP | NuCare Pharmaceuticals,Inc. | 2025-06-09 | HUMAN PRESCRIPTION DRUG LABEL | 3 |