# AZITHROMYCIN DIHYDRATE

NDC: 72189-090
Generic name: AZITHROMYCIN DIHYDRATE
Labeler / Manufacturer: DIRECT RX
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20200522
Marketing ended: 20261031
FDA application: ANDA208249

## Active ingredients

- AZITHROMYCIN DIHYDRATE: 500 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72189-090"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72189-090
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a6426d5f-5518-3c69-e053-2995a90af50f