NDC 76519-1005
Lamivudine and Zidovudine 150 mg / 300 mg tablet, film coated
On the label: H.J. Harkins Co., Inc.. It's repackaged from NDC 0093-5385, made by Teva Pharmaceuticals USA, Inc. (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. 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 H.J. Harkins Co., Inc. names for other drugs.
Product details
- Generic drug
- Lamivudine and Zidovudine: every company that makes it
- Form
- tablet, film coated
- Strength
- 150 mg / 300 mg
- Approval
- ANDA ANDA079081
- On the market since
- Dec 27, 2011
- Package NDCs
76519-1005-6- Official label
- DailyMed (National Library of Medicine), updated Jun 25, 2012
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