Package 71610-979-80

Brand: memantine hydrochloride

Generic: memantine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71610-979-80
Digits Only 7161097980
Product NDC 71610-979
Product ID 71610-979_47e4a650-9483-bc12-e063-6294a90a695d
Description

180 TABLET, FILM COATED in 1 BOTTLE (71610-979-80)

Marketing

Marketing Status
Marketed Since 2026-01-08
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": "47e4a650-9483-bc12-e063-6294a90a695d", "openfda": {"unii": ["JY0WD0UA60"], "rxcui": ["996571"], "spl_set_id": ["47e4a696-fe2a-c905-e063-6294a90a7415"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (71610-979-80)", "package_ndc": "71610-979-80", "marketing_start_date": "20260108"}], "brand_name": "Memantine Hydrochloride", "product_id": "71610-979_47e4a650-9483-bc12-e063-6294a90a695d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["N-methyl-D-aspartate Receptor Antagonist [EPC]", "NMDA Receptor Antagonists [MoA]"], "product_ndc": "71610-979", "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": "5 mg/1"}], "application_number": "ANDA200022", "marketing_category": "ANDA", "marketing_start_date": "20151101", "listing_expiration_date": "20271231"}