# Clopidogrel

NDC: 68071-4138
Generic name: Clopidogrel
Labeler / Manufacturer: NuCare Pharmaceuticals,Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20120517

FDA application: ANDA076999

## Active ingredients

- CLOPIDOGREL BISULFATE: 75 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68071-4138"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68071-4138
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5cdca9bd-7042-142a-e053-2991aa0a9ca6