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Omeprazole

NDC 76420-879 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE

Labeler / ManufacturerAsclemed USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA091672
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsOMEPRAZOLE (40 mg/1)
Marketing started20141031
Package count6

External sources

Source: openFDA. Public-domain (CC0).