Sunitinib malate
- Product NDC
- 63304-091
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sunitinib malate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Sun Pharmaceutical Industries Inc.
- Application
- ANDA213914
- Marketing category
- ANDA
- Substance
- SUNITINIB MALATE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 63304-091-27 | 28 CAPSULE in 1 BOTTLE (63304-091-27) | 2019-12-25 | | No | Historical |
| 63304-091-86 | 4 BLISTER PACK in 1 BOX (63304-091-86) / 7 CAPSULE in 1 BLISTER PACK (63304-091-11) | 2019-12-25 | | No | Historical |