NDC 66116-518
Ranitidine 150 mg tablet, film coated
On the label: MedVantx, Inc.. It's repackaged from NDC 0172-4357, made by Teva Pharmaceuticals USA, Inc. (Ranitidine). 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). 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 MedVantx, Inc. names for other drugs.
Product details
- Generic drug
- Ranitidine: every company that makes it
- Form
- tablet, film coated
- Strength
- 150 mg
- Approval
- ANDA ANDA075165
- On the market since
- Sep 12, 1997
- Package NDCs
66116-518-60- Official label
- DailyMed (National Library of Medicine), updated Aug 30, 2012
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