Package 63629-2512-1
Brand: memantine hydrochloride
Generic: memantine hydrochloridePackage Facts
Identity
Package NDC
63629-2512-1
Digits Only
6362925121
Product NDC
63629-2512
Description
60 TABLET in 1 BOTTLE (63629-2512-1)
Marketing
Marketing Status
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": "f05f0498-106d-45f5-9509-dcbd3a25d062", "openfda": {"unii": ["JY0WD0UA60"], "rxcui": ["996561"], "spl_set_id": ["c8f96b24-de66-4a17-b798-42b42a25e84c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (63629-2512-1)", "package_ndc": "63629-2512-1", "marketing_start_date": "20210518"}], "brand_name": "Memantine Hydrochloride", "product_id": "63629-2512_f05f0498-106d-45f5-9509-dcbd3a25d062", "dosage_form": "TABLET", "pharm_class": ["N-methyl-D-aspartate Receptor Antagonist [EPC]", "NMDA Receptor Antagonists [MoA]"], "product_ndc": "63629-2512", "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"}