# Azithromycin

NDC: 50111-789
Generic name: Azithromycin
Labeler / Manufacturer: Teva Pharmaceuticals USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20051201

FDA application: ANDA065218

## Active ingredients

- AZITHROMYCIN MONOHYDRATE: 600 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50111-789"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50111-789
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ac549022-4d7f-4c9f-9244-1a2df9a27276