# Azathioprine Sodium

NDC: 0143-9566
Generic name: Azathioprine Sodium
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 19950501

FDA application: ANDA074419

## Active ingredients

- AZATHIOPRINE SODIUM: 100 mg/10mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0143-9566"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0143-9566
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9ffe79a1-ac91-4a7b-a9e3-7c84bfa9ddf0