# Clopidogrel Bisulfate

NDC: 47335-894
Generic name: Clopidogrel Bisulfate
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20120518

FDA application: ANDA090494

## Active ingredients

- CLOPIDOGREL BISULFATE: 75 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"47335-894"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=47335-894
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d37db064-3a5a-4a0c-a60b-b4b417fe742a