Package 72603-118-01

Brand: memantine

Generic: memantine
NDC Package

Package Facts

Identity

Package NDC 72603-118-01
Digits Only 7260311801
Product NDC 72603-118
Product ID 72603-118_dd10c9a1-a7af-b51f-4317-ee2290f19a85
Description

60 TABLET in 1 BOTTLE (72603-118-01)

Marketing

Marketing Status
Marketed Since 2022-09-13
Brand memantine
Generic memantine
Sample Package No

Linked Drug Pages (1)

Memantine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "dd10c9a1-a7af-b51f-4317-ee2290f19a85", "openfda": {"unii": ["JY0WD0UA60"], "rxcui": ["996561", "996571"], "spl_set_id": ["7a40ed9d-8853-b616-ff47-0c7b0fd28959"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (72603-118-01)", "package_ndc": "72603-118-01", "marketing_start_date": "20220913"}], "brand_name": "Memantine", "product_id": "72603-118_dd10c9a1-a7af-b51f-4317-ee2290f19a85", "dosage_form": "TABLET", "pharm_class": ["N-methyl-D-aspartate Receptor Antagonist [EPC]", "NMDA Receptor Antagonists [MoA]"], "product_ndc": "72603-118", "generic_name": "Memantine", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Memantine", "active_ingredients": [{"name": "MEMANTINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA090048", "marketing_category": "ANDA", "marketing_start_date": "20220913", "listing_expiration_date": "20261231"}