Quetiapine
- Product NDC
- 55154-8092
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Quetiapine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cardinal Health 107, LLC
- Application
- ANDA201504
- Marketing category
- ANDA
- Substance
- QUETIAPINE FUMARATE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 55154-8092-0 | 10 BLISTER PACK in 1 BAG (55154-8092-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK | 2013-03-01 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| These highlights do not include all the information needed to use QUETIAPINE TABLETS safely and effectively. See full prescribing information for QUETIAPINE TABLETS. QUETIAPINE tablets, for oral use Initial U.S. Approval: 1997 | Cardinal Health 107, LLC | 2026-01-15 | HUMAN PRESCRIPTION DRUG LABEL | 12 |