# Azathioprine

NDC: 68462-502
Generic name: Azathioprine
Labeler / Manufacturer: Glenmark Pharmaceuticals, Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 19990801

FDA application: ANDA075252

## Active ingredients

- AZATHIOPRINE: 50 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68462-502"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68462-502
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ceab8e8b-d022-4d0c-a552-cc5782446248