# Sunitinib malate

NDC: 16714-676
Generic name: Sunitinib malate
Labeler / Manufacturer: NorthStar RxLLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20220218

FDA application: ANDA213914

## Active ingredients

- SUNITINIB MALATE: 12.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"16714-676"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16714-676
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7579e3d0-2de6-4239-a7a8-118ed92075f5