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MEMANTINE HYDROCHLORIDE

NDC 59651-404 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA214651
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsMEMANTINE HYDROCHLORIDE (7 mg/1)
Marketing started20210809
Package count2

External sources

Source: openFDA. Public-domain (CC0).