Quetiapine fumarate
- Product NDC
- 47335-907
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Quetiapine fumarate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Application
- ANDA201190
- Marketing category
- ANDA
- Substance
- QUETIAPINE FUMARATE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 47335-907-18 | 1000 TABLET, FILM COATED in 1 BOTTLE (47335-907-18) | 2012-03-28 | | No | Historical |
| 47335-907-61 | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (47335-907-61) / 10 TABLET, FILM COATED in 1 BLISTER PACK | 2012-03-28 | | No | Historical |
| 47335-907-83 | 30 TABLET, FILM COATED in 1 BOTTLE (47335-907-83) | 2012-03-28 | | No | Historical |
| 47335-907-88 | 100 TABLET, FILM COATED in 1 BOTTLE (47335-907-88) | 2012-03-28 | | No | Historical |