# eltrombopag

NDC: 43598-151
Generic name: eltrombopag
Labeler / Manufacturer: Dr. Reddy's Laboratories Inc.,
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20260317

FDA application: ANDA219121

## Active ingredients

- ELTROMBOPAG OLAMINE: 12.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43598-151"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43598-151
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e5fd3114-56b8-3ae3-fb03-9820a26ca4c6