# CLOPIDOGREL BISULFATE

NDC: 64980-713
Generic name: CLOPIDOGREL BISULFATE
Labeler / Manufacturer: Rising Pharma Holdings, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20261015

FDA application: ANDA204359

## 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:"64980-713"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=64980-713