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memantine hydrochloride

NDC 0904-6734 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA206028
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsMEMANTINE HYDROCHLORIDE (7 mg/1)
Marketing started20180220
Package count1

External sources

Source: openFDA. Public-domain (CC0).