Desvenlafaxine Succinate
- Product NDC
- 68180-604
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Desvenlafaxine Succinate
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Lupin Pharmaceuticals, Inc.
- Application
- ANDA204172
- Marketing category
- ANDA
- Substance
- DESVENLAFAXINE SUCCINATE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 68180-604-06 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68180-604-06) | 2022-08-25 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| Desvenlafaxine Succinate | Bryant Ranch Prepack | 2026-05-08 | HUMAN PRESCRIPTION DRUG LABEL | 2 |
| Desvenlafaxine Succinate | Lupin Pharmaceuticals, Inc. | LUPIN LIMITED | 2025-12-29 | HUMAN PRESCRIPTION DRUG LABEL | 23 |
| Desvenlafaxine Succinate | A-S Medication Solutions | 2024-12-05 | HUMAN PRESCRIPTION DRUG LABEL | 1 |