# SUNITINIB MALATE

NDC: 43598-047
Generic name: SUNITINIB MALATE
Labeler / Manufacturer: Dr.Reddys Laboratories Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20221130

FDA application: ANDA215843

## Active ingredients

- SUNITINIB MALATE: 37.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43598-047"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43598-047
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=96ce8850-b5ae-382b-8433-04949533af44