NDC 42708-170
Omeprazole 20 mg capsule, delayed release
On the label: QPharma, Inc.. It's repackaged: QPharma, Inc. rebottles it from Sandoz Inc.'s NDC 0781-2868.
Where the pills inside were made
This label doesn't name the factory that makes the drug. 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 Sandoz Inc. names for other drugs.
Product details
- Generic drug
- Omeprazole: every company that makes it
- Form
- capsule, delayed release, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA075757
- On the market since
- Jul 1, 2019
- Package NDCs
42708-170-14- Official label
- DailyMed (National Library of Medicine), updated May 11, 2026
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