NDC 50436-2852
Azithromycin Dihydrate 500 mg tablet, film coated
On the label: Unit Dose Services.
It's a repackaged product (source NDC 60505-2582, which isn't on a current label).
Where it's made
This label doesn't name the factory that makes the drug (it lists 1 site that repackages it and relabels it). Companies aren't required to print it on the label. The manufacturer's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Unit Dose Services uses for other drugs.
Product details
- Generic drug
- Azithromycin: see every company that makes it
- Form
- tablet, film coated
- Strength
- 500 mg
- Approval
- ANDA ANDA065509
- On the market since
- Jul 18, 2011
- Package NDCs
50436-2852-150436-2852-2- Official label
- DailyMed (National Library of Medicine), updated May 15, 2018
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?