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Esomeprazole Magnesium

NDC 68462-390 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE PELLETS

Labeler / ManufacturerGlenmark Pharmaceuticals Inc., USA
Marketing categoryAbbreviated NDA (generic) · App ANDA209495
Dosage form / routeCAPSULE, DELAYED RELEASE PELLETS · ORAL
Active ingredientsESOMEPRAZOLE MAGNESIUM (20 mg/1)
Marketing started20211101
Package count3

External sources

Source: openFDA. Public-domain (CC0).