Package 55154-4151-0

Brand: memantine hydrochloride

Generic: memantine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 55154-4151-0
Digits Only 5515441510
Product NDC 55154-4151
Description

10 BLISTER PACK in 1 BAG (55154-4151-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2022-05-12
Brand memantine hydrochloride
Generic memantine hydrochloride
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2104a25e-845b-4bea-8a82-5274b878961f", "openfda": {"upc": ["0055154763707", "0055154415101"], "unii": ["JY0WD0UA60"], "rxcui": ["996561", "996571"], "spl_set_id": ["65c9e7bc-71f0-4113-8de1-4fcaa591735f"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-4151-0)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "55154-4151-0", "marketing_start_date": "20220512"}], "brand_name": "Memantine Hydrochloride", "product_id": "55154-4151_2104a25e-845b-4bea-8a82-5274b878961f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["N-methyl-D-aspartate Receptor Antagonist [EPC]", "NMDA Receptor Antagonists [MoA]"], "product_ndc": "55154-4151", "generic_name": "Memantine Hydrochloride", "labeler_name": "Cardinal Health 107, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Memantine Hydrochloride", "active_ingredients": [{"name": "MEMANTINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA090048", "marketing_category": "ANDA", "marketing_start_date": "20150720", "listing_expiration_date": "20271231"}