Package 71610-885-80

Brand: memantine hydrochloride

Generic: memantine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71610-885-80
Digits Only 7161088580
Product NDC 71610-885
Product ID 71610-885_30b8a715-b7de-66fc-e063-6394a90a4e76
Description

180 TABLET in 1 BOTTLE (71610-885-80)

Marketing

Marketing Status
Marketed Since 2025-03-18
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": "30b8a715-b7de-66fc-e063-6394a90a4e76", "openfda": {"unii": ["JY0WD0UA60"], "rxcui": ["996561"], "spl_set_id": ["30b8b982-db74-7cf4-e063-6394a90a3a6b"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET in 1 BOTTLE (71610-885-80)", "package_ndc": "71610-885-80", "marketing_start_date": "20250318"}], "brand_name": "Memantine Hydrochloride", "product_id": "71610-885_30b8a715-b7de-66fc-e063-6394a90a4e76", "dosage_form": "TABLET", "pharm_class": ["N-methyl-D-aspartate Receptor Antagonist [EPC]", "NMDA Receptor Antagonists [MoA]"], "product_ndc": "71610-885", "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": "ANDA206528", "marketing_category": "ANDA", "marketing_start_date": "20150827", "listing_expiration_date": "20261231"}