NDC 50436-1720
Prednisone 5 mg tablet
On the label: Unit Dose Services.
It's a repackaged product (source NDC 59746-172, 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
- Prednisone: see every company that makes it
- Form
- tablet
- Strength
- 5 mg
- Approval
- ANDA ANDA040362
- On the market since
- Aug 29, 2001
- Package NDCs
50436-1720-150436-1720-450436-1720-5- Official label
- DailyMed (National Library of Medicine), updated May 13, 2019
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?