# abiraterone acetate

NDC: 68462-135
Generic name: abiraterone acetate
Labeler / Manufacturer: Glenmark Pharmaceuticals Inc., USA
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20191016

FDA application: ANDA209227

## Active ingredients

- ABIRATERONE ACETATE: 250 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68462-135"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68462-135
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ba32c453-a231-452a-a6d9-b3e57afb2e75