# Zithromax

NDC: 0069-3130
Generic name: azithromycin dihydrate
Labeler / Manufacturer: Pfizer Laboratories Div Pfizer Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: POWDER, FOR SUSPENSION
Routes: ORAL
Marketing started: 19951019

FDA application: NDA050710

## Active ingredients

- AZITHROMYCIN DIHYDRATE: 200 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0069-3130"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0069-3130
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=db52b91e-79f7-4cc1-9564-f2eee8e31c45