FDA NDC Directory · JSON-LD · Markdown

omeprazole

NDC 57483-740 · HUMAN OTC DRUG · CAPSULE, DELAYED RELEASE

Labeler / ManufacturerINNOVUS PHARMACEUTICALS, INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA210593
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsOMEPRAZOLE MAGNESIUM (20.6 mg/1)
Marketing started20200806
Package count1

External sources

Source: openFDA. Public-domain (CC0).