NDC 50436-3136
azithromycin monohydrate 500 mg tablet
On the label: Unit Dose Services. It's repackaged from NDC 68180-161, made by Lupin Pharmaceuticals, Inc. (azithromycin monohydrate). 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 Unit Dose Services names for other drugs.
Product details
- Generic drug
- Azithromycin: every company that makes it
- Form
- tablet
- Strength
- 500 mg
- Approval
- ANDA ANDA065399
- On the market since
- Aug 18, 2015
- Package NDCs
50436-3136-350436-3136-4- Official label
- DailyMed (National Library of Medicine), updated Aug 15, 2017
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