Quetiapine
- Product NDC
- 71610-702
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Quetiapine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA077745
- Marketing category
- ANDA
- Substance
- QUETIAPINE FUMARATE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71610-702-15 | 15 TABLET, FILM COATED in 1 BOTTLE (71610-702-15) | 2023-04-18 | | No | Historical |
| 71610-702-30 | 30 TABLET, FILM COATED in 1 BOTTLE (71610-702-30) | 2023-04-18 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Quetiapine | Aphena Pharma Solutions - Tennessee, LLC | 2023-04-19 | HUMAN PRESCRIPTION DRUG LABEL | 1 |