FDA NDC Directory · JSON-LD · Markdown

Esomeprazole Magnesium

NDC 62175-820 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE PELLETS

Labeler / ManufacturerLannett Company, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA205563
Dosage form / routeCAPSULE, DELAYED RELEASE PELLETS · ORAL
Active ingredientsESOMEPRAZOLE MAGNESIUM (20 mg/1)
Marketing started20170901
Package count3

External sources

Source: openFDA. Public-domain (CC0).