Package 50090-6291-1

Brand: memantine hydrochloride

Generic: memantine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-6291-1
Digits Only 5009062911
Product NDC 50090-6291
Description

90 TABLET in 1 BOTTLE (50090-6291-1)

Marketing

Marketing Status
Marketed Since 2022-12-21
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": "eb840a53-9a53-42d8-b4ac-c02fd35d3bc7", "openfda": {"unii": ["JY0WD0UA60"], "rxcui": ["996571"], "spl_set_id": ["f05e381f-850d-42ea-9dd8-6d1f8dac4f62"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-6291-0)", "package_ndc": "50090-6291-0", "marketing_start_date": "20221221"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-6291-1)", "package_ndc": "50090-6291-1", "marketing_start_date": "20221221"}], "brand_name": "Memantine Hydrochloride", "product_id": "50090-6291_eb840a53-9a53-42d8-b4ac-c02fd35d3bc7", "dosage_form": "TABLET", "pharm_class": ["N-methyl-D-aspartate Receptor Antagonist [EPC]", "NMDA Receptor Antagonists [MoA]"], "product_ndc": "50090-6291", "generic_name": "Memantine Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Memantine Hydrochloride", "active_ingredients": [{"name": "MEMANTINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA090961", "marketing_category": "ANDA", "marketing_start_date": "20190228", "listing_expiration_date": "20261231"}