NDC 50436-0117
cephalexin 500 mg capsule
On the label: Unit Dose Services.
It's a repackaged product: Unit Dose Services rebottles it from Sun Pharmaceutical Industries Limited's NDC 62756-294.
Where the pills inside were made
This label doesn't name the factory that makes the drug. 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 Sun Pharmaceutical Industries Limited uses for other drugs.
Repackaging site
- Unit Dose Services, · repackages it
Recalls
- Jun 26, 2014 · Class II · Terminated
CGMP Deviations: These products are being recalled because they were manufactured with active pharmaceutical ingredients (APIs) that were not manufactured with good manufacturing practices.
Lots: Lot #: a) AGL0058B, AGL0059B, AGL0060B, AGL0061B, Exp 06/14; AGL0062B, AGL0063B, AGL0064B, Exp 07/14; AGL0083B, AGL0084B, AGL0085B, AGL0086B, AGL0087B, AGL0088B, AGL0089B, AGL0090B, Exp 08/14; AGL0120B, AGL0121B, AGL0122B, AGL0123B, Exp 11/14; AGM0001B, AGM0002B, AGM0003B, AGM0004B, Exp 12/14; AGM0…
Product details
- Generic drug
- Cephalexin: see every company that makes it
- Form
- capsule
- Strength
- 500 mg
- Approval
- ANDA ANDA062791
- On the market since
- Jun 21, 2010
- Package NDCs
50436-0117-150436-0117-250436-0117-350436-0117-450436-0117-550436-0117-8- Official label
- DailyMed (National Library of Medicine), updated Jun 14, 2010
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?