NDC 61919-061
Lamivudine Zidovudine 150 mg / 300 mg tablet
On the label: Direct Rx. It's repackaged from NDC 65862-597, made by Aurobindo Pharma Limited (Lamivudine and Zidovudine). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were made
This label doesn't name the factory that makes the drug (it lists 1 site that repackages it and relabels it). 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 Direct Rx names for other drugs.
Product details
- Generic drug
- Lamivudine and Zidovudine: every company that makes it
- Form
- tablet
- Strength
- 150 mg / 300 mg
- Approval
- ANDA ANDA202418
- On the market since
- Jan 1, 2015
- Package NDCs
61919-061-02- Official label
- DailyMed (National Library of Medicine), updated Jun 22, 2016
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?