NDC 43063-900
LAMIVUDINE and ZIDOVUDINE 150 mg / 300 mg tablet, film coated
On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from Camber Pharmaceuticals Inc.'s NDC 31722-506.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hetero Labs Limited | Hyderabad, India | Makes it | Problems found, fixed voluntarilyJul 21, 2023 · 8 inspections |
| Hetero Labs Limited | Mahabubnagar, India | Makes it | Problems found, fixed voluntarilyAug 12, 2022 · 5 inspections, 1 with FDA action |
Repackaging site
- PD-Rx Pharmaceuticals Inc., Oklahoma City, OK, United States · repackages it
Product details
- Generic drug
- Lamivudine and Zidovudine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 150 mg / 300 mg
- Approval
- ANDA ANDA079124
- On the market since
- Sep 18, 2015
- Package NDCs
43063-900-06- Official label
- DailyMed (National Library of Medicine), updated Oct 17, 2025
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