Package 71610-011-18

Brand: memantine hydrochloride

Generic: memantine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71610-011-18
Digits Only 7161001118
Product NDC 71610-011
Product ID 71610-011_f384e3d8-d9fd-481c-b924-4bf98dfb5bdf
Description

3000 TABLET in 1 BOTTLE (71610-011-18)

Marketing

Marketing Status
Marketed Since 2017-11-15
Brand memantine hydrochloride
Generic memantine hydrochloride
Sample Package No

Linked Drug Pages (1)

memantine hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f384e3d8-d9fd-481c-b924-4bf98dfb5bdf", "openfda": {"unii": ["JY0WD0UA60"], "rxcui": ["996561"], "spl_set_id": ["c8f5c20b-4573-44c5-89fc-4da11b2e1fe1"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "3000 TABLET in 1 BOTTLE (71610-011-18)", "package_ndc": "71610-011-18", "marketing_start_date": "20171115"}], "brand_name": "memantine hydrochloride", "product_id": "71610-011_f384e3d8-d9fd-481c-b924-4bf98dfb5bdf", "dosage_form": "TABLET", "pharm_class": ["N-methyl-D-aspartate Receptor Antagonist [EPC]", "NMDA Receptor Antagonists [MoA]"], "product_ndc": "71610-011", "generic_name": "memantine hydrochloride", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "memantine hydrochloride", "active_ingredients": [{"name": "MEMANTINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "NDA021487", "marketing_category": "NDA", "marketing_start_date": "20150401", "listing_expiration_date": "20261231"}