Package 70518-3338-1

Brand: memantine hydrochloride

Generic: memantine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3338-1
Digits Only 7051833381
Product NDC 70518-3338
Description

60 TABLET in 1 BOTTLE, PLASTIC (70518-3338-1)

Marketing

Marketing Status
Marketed Since 2025-05-28
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": "36462b8b-8138-11a0-e063-6394a90ad027", "openfda": {"unii": ["JY0WD0UA60"], "rxcui": ["996571"], "spl_set_id": ["cbfd9d95-f50b-45ff-9857-9f1712c45e56"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (70518-3338-1)", "package_ndc": "70518-3338-1", "marketing_start_date": "20250528"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-3338-2)", "package_ndc": "70518-3338-2", "marketing_start_date": "20250528"}], "brand_name": "Memantine Hydrochloride", "product_id": "70518-3338_36462b8b-8138-11a0-e063-6394a90ad027", "dosage_form": "TABLET", "pharm_class": ["N-methyl-D-aspartate Receptor Antagonist [EPC]", "NMDA Receptor Antagonists [MoA]"], "product_ndc": "70518-3338", "generic_name": "Memantine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "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": "20220120", "listing_expiration_date": "20261231"}