NDC 55695-003
Azithromycin 200 mg per 5 mL powder, for suspension
On the label: Department of State Health Services, Pharmacy Branch. It's repackaged: Department of State Health Services, Pharmacy Branch rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 0093-2026.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Teva Pharmaceuticals USA, Inc. names for other drugs.
Product details
- Generic drug
- Azithromycin: every company that makes it
- Form
- powder, for suspension, oral
- Strength
- 200 mg per 5 mL
- Approval
- ANDA ANDA065246
- On the market since
- Dec 17, 2010
- Package NDCs
55695-003-0055695-003-01- Official label
- DailyMed (National Library of Medicine), updated Feb 29, 2024
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