FDA NDC Directory · JSON-LD · Markdown

Omeprazole

NDC 70677-0148 · HUMAN OTC DRUG · TABLET, DELAYED RELEASE

Labeler / ManufacturerStrategic Sourcing Services
Marketing categoryAbbreviated NDA (generic) · App ANDA207891
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsOMEPRAZOLE (20 mg/1)
Marketing started20190101
Package count1

External sources

Source: openFDA. Public-domain (CC0).