Package 67046-1471-3

Brand: memantine hydrochloride

Generic: memantine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67046-1471-3
Digits Only 6704614713
Product NDC 67046-1471
Product ID 67046-1471_2d54b58a-d1dc-e87f-e063-6394a90ab92e
Description

30 TABLET in 1 BLISTER PACK (67046-1471-3)

Marketing

Marketing Status
Marketed Since 2025-02-04
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": "2d54b58a-d1dc-e87f-e063-6394a90ab92e", "openfda": {"unii": ["JY0WD0UA60"], "rxcui": ["996571"], "spl_set_id": ["2d54be77-75b2-76b3-e063-6294a90a0cc0"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (67046-1471-3)", "package_ndc": "67046-1471-3", "marketing_start_date": "20250204"}], "brand_name": "Memantine Hydrochloride", "product_id": "67046-1471_2d54b58a-d1dc-e87f-e063-6394a90ab92e", "dosage_form": "TABLET", "pharm_class": ["N-methyl-D-aspartate Receptor Antagonist [EPC]", "NMDA Receptor Antagonists [MoA]"], "product_ndc": "67046-1471", "generic_name": "Memantine Hydrochloride", "labeler_name": "Coupler LLC", "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": "20250204", "listing_expiration_date": "20261231"}