# Clopidogrel bisulfate

NDC: 82009-182
Generic name: Clopidogrel bisulfate
Labeler / Manufacturer: Quallent Pharmaceuticals Health LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20250905

FDA application: ANDA091023

## 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:"82009-182"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=82009-182
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d072b6ea-2bb4-8965-918e-23f9080efcb0