NDC 50436-3125
Omeprazole 20 mg capsule, delayed release
On the label: Unit Dose Services.
It's a repackaged product: Unit Dose Services rebottles it from Lannett Company, Inc.'s NDC 62175-118.
Where the pills inside were made
This label doesn't name the factory that makes the drug (it lists 1 site that packages it and labels 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 Lannett Company, Inc. uses for other drugs.
Repackaging site
- Unit Dose Services, · repackages it and relabels it
Recalls
- Sep 16, 2013 · Class II · Terminated
Failed Tablet/Capsule Specification: some capsules over time do not meet or are suspected to not meet the specification for acid resistance.
Lots: Lot Number 59627; Expiration Date 02/2014
Product details
- Generic drug
- Omeprazole: see every company that makes it
- Form
- capsule, delayed release
- Strength
- 20 mg
- Approval
- ANDA ANDA075410
- On the market since
- Nov 4, 2002
- Package NDCs
50436-3125-150436-3125-250436-3125-3- Official label
- DailyMed (National Library of Medicine), updated Jul 1, 2017
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?