Package 63629-2514-1

Brand: memantine hydrochloride

Generic: memantine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-2514-1
Digits Only 6362925141
Product NDC 63629-2514
Description

60 TABLET in 1 BOTTLE (63629-2514-1)

Marketing

Marketing Status
Marketed Since 2021-05-18
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": "16652984-6db6-4780-9fa8-8faf436c404c", "openfda": {"unii": ["JY0WD0UA60"], "rxcui": ["996571"], "spl_set_id": ["fac8c59b-5bf5-478e-8223-a5ecaa400625"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (63629-2514-1)", "package_ndc": "63629-2514-1", "marketing_start_date": "20210518"}], "brand_name": "Memantine Hydrochloride", "product_id": "63629-2514_16652984-6db6-4780-9fa8-8faf436c404c", "dosage_form": "TABLET", "pharm_class": ["N-methyl-D-aspartate Receptor Antagonist [EPC]", "NMDA Receptor Antagonists [MoA]"], "product_ndc": "63629-2514", "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": "5 mg/1"}], "application_number": "ANDA090961", "marketing_category": "ANDA", "marketing_start_date": "20190228", "listing_expiration_date": "20261231"}