Package 68180-229-07

Brand: memantine hydrochloride

Generic: memantine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68180-229-07
Digits Only 6818022907
Product NDC 68180-229
Description

60 TABLET, FILM COATED in 1 BOTTLE (68180-229-07)

Marketing

Marketing Status
Marketed Since 2015-07-13
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": "392d48fd-7c93-40f3-9ab0-d0f304b7e439", "openfda": {"upc": ["0368180230076", "0368180229070"], "unii": ["JY0WD0UA60"], "rxcui": ["996561", "996571"], "spl_set_id": ["1b4a0162-9cb4-4ba6-8c02-95c2955734ae"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68180-229-07)", "package_ndc": "68180-229-07", "marketing_start_date": "20150713"}], "brand_name": "Memantine hydrochloride", "product_id": "68180-229_392d48fd-7c93-40f3-9ab0-d0f304b7e439", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["N-methyl-D-aspartate Receptor Antagonist [EPC]", "NMDA Receptor Antagonists [MoA]"], "product_ndc": "68180-229", "generic_name": "Memantine hydrochloride", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Memantine hydrochloride", "active_ingredients": [{"name": "MEMANTINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA090051", "marketing_category": "ANDA", "marketing_start_date": "20150713", "listing_expiration_date": "20261231"}