NDC 0069-3051
Zithromax 1 g powder, for suspension
On the label: Pfizer Laboratories Div Pfizer Inc.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Pfizer Asia Manufacturing Pte Ltd | Singapore, Singapore | Makes the active ingredient and tests it | Problems found, fixed voluntarilyOct 18, 2023 · 6 inspections |
| Pfizer Ireland Pharmaceuticals Unlimited Company | Ringaskiddy, Ireland | Makes the active ingredient and tests it | Problems found, fixed voluntarilyOct 25, 2024 · 6 inspections |
| Eurofins Lancaster Laboratories, LLC | Lancaster, PA, United States | Tests it | Problems found, fixed voluntarilyAug 26, 2025 · 8 inspections |
| Pfizer Inc | Location not on file | Tests it | Not inspected on record |
| Viatris Pharmaceuticals LLC | Vega Baja, PR, United States | Tests it and packages it | Problems found, fixed voluntarilyMay 18, 2026 · 11 inspections |
Product details
- Generic drug
- Azithromycin: every company that makes it
- Form
- powder, for suspension
- Strength
- 1 g
- Approval
- NDA NDA050693
- On the market since
- Sep 28, 1994
- Package NDCs
0069-3051-010069-3051-75- Official label
- DailyMed (National Library of Medicine), updated Sep 5, 2025
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