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Lansoprazole

NDC 63187-152 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA077255
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsLANSOPRAZOLE (30 mg/1)
Marketing started20091111
Package count1

External sources

Source: openFDA. Public-domain (CC0).