Package 50268-587-13

Brand: memantine hydrochloride

Generic: memantine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50268-587-13
Digits Only 5026858713
Product NDC 50268-587
Description

30 BLISTER PACK in 1 BOX (50268-587-13) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-587-11)

Marketing

Marketing Status
Marketed Since 2024-02-20
Brand memantine hydrochloride
Generic memantine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47e7cea9-cd6c-40d4-e063-6294a90a9e8a", "openfda": {"unii": ["JY0WD0UA60"], "rxcui": ["996561", "996571"], "spl_set_id": ["11d27c75-fdc0-f9da-e063-6394a90ac6b0"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 BOX (50268-587-13)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-587-11)", "package_ndc": "50268-587-13", "marketing_start_date": "20240220"}], "brand_name": "Memantine Hydrochloride", "product_id": "50268-587_47e7cea9-cd6c-40d4-e063-6294a90a9e8a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["N-methyl-D-aspartate Receptor Antagonist [EPC]", "NMDA Receptor Antagonists [MoA]"], "product_ndc": "50268-587", "generic_name": "memantine hydrochloride", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Memantine Hydrochloride", "active_ingredients": [{"name": "MEMANTINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA200022", "marketing_category": "ANDA", "marketing_start_date": "20240220", "listing_expiration_date": "20271231"}