FDA NDC Directory · JSON-LD · Markdown

Memantine hydrochloride

NDC 33342-220 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Labeler / ManufacturerMacleods Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA206310
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsMEMANTINE HYDROCHLORIDE (14 mg/1)
Marketing started20250828
Package count2

External sources

Source: openFDA. Public-domain (CC0).