NDC 53808-0812
Zidovudine 300 mg tablet, film coated
On the label: State of Florida DOH Central Pharmacy. It's repackaged: State of Florida DOH Central Pharmacy rebottles it from Aurobindo Pharma Limited's NDC 65862-024.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action |
| Aurobindo Pharma Limited | Mahabubnagar, India | Makes it and tests it | Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action |
Repackaging site
- State of Florida DOH Central Pharmacy, Location not on file · repackages it
Product details
- Generic drug
- Zidovudine: every company that makes it
- Form
- tablet, film coated
- Strength
- 300 mg
- Approval
- ANDA ANDA077267
- On the market since
- Jul 1, 2009
- Package NDCs
53808-0812-1- Official label
- DailyMed (National Library of Medicine), updated Jan 20, 2017
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