# Azithromycin monohydrate

NDC: 70095-025
Generic name: Azithromycin monohydrate
Labeler / Manufacturer: Sun Pharmaceutical Industries Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20230327

FDA application: ANDA065501

## Active ingredients

- AZITHROMYCIN MONOHYDRATE: 500 mg/10mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70095-025"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70095-025
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c8d012c4-f411-4484-a618-7597599ea621