# Zithromax

NDC: 0069-3150
Generic name: azithromycin dihydrate
Labeler / Manufacturer: Pfizer Laboratories Div Pfizer Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 19970130

FDA application: NDA050733

## Active ingredients

- AZITHROMYCIN DIHYDRATE: 500 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0069-3150"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0069-3150
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3b631aa1-2d46-40bc-a614-d698301ea4f9