Package 72162-2004-5

Brand: memantine hydrochloride

Generic: memantine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2004-5
Digits Only 7216220045
Product NDC 72162-2004
Description

500 TABLET in 1 BOTTLE (72162-2004-5)

Marketing

Marketing Status
Marketed Since 2024-02-06
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": "41c04bd6-b745-4e94-a9ce-5b3babcd2039", "openfda": {"unii": ["JY0WD0UA60"], "rxcui": ["996561"], "spl_set_id": ["be919d34-e9f4-49c8-8145-2dcafb7cb88c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (72162-2004-5)", "package_ndc": "72162-2004-5", "marketing_start_date": "20240206"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (72162-2004-6)", "package_ndc": "72162-2004-6", "marketing_start_date": "20240206"}], "brand_name": "Memantine Hydrochloride", "product_id": "72162-2004_41c04bd6-b745-4e94-a9ce-5b3babcd2039", "dosage_form": "TABLET", "pharm_class": ["N-methyl-D-aspartate Receptor Antagonist [EPC]", "NMDA Receptor Antagonists [MoA]"], "product_ndc": "72162-2004", "generic_name": "Memantine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Memantine Hydrochloride", "active_ingredients": [{"name": "MEMANTINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA090961", "marketing_category": "ANDA", "marketing_start_date": "20190228", "listing_expiration_date": "20261231"}