NDC 67296-0882

Omeprazole 20 mg capsule, delayed release

On the label: RedPharm Drug. Inc.. It's a repackaged product: RedPharm Drug. Inc. rebottles it from Apotex Corp.'s NDC 60505-0065.

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 Apotex Corp. uses for other drugs.

Repackaging site

Product details

Generic drug
Omeprazole: see every company that makes it
Form
capsule, delayed release
Strength
20 mg
Approval
ANDA ANDA076048
On the market since
Nov 11, 2003
Package NDCs
67296-0882-1 67296-0882-2
Official label
DailyMed (National Library of Medicine), updated Jan 20, 2020

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