NDC 65862-036
Lamivudine and Zidovudine 150 mg / 300 mg tablet, film coated
On the label: Aurobindo Pharma Limited.
Where it's 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 |
Product details
- Generic drug
- Lamivudine and Zidovudine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 150 mg / 300 mg
- Approval
- ANDA ANDA077558
- On the market since
- May 5, 2017
- Package NDCs
65862-036-1065862-036-60- Official label
- DailyMed (National Library of Medicine), updated May 24, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?