Package 60687-173-57

Brand: memantine

Generic: memantine
NDC Package

Package Facts

Identity

Package NDC 60687-173-57
Digits Only 6068717357
Product NDC 60687-173
Description

60 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-173-57) / 1 TABLET in 1 BLISTER PACK (60687-173-11)

Marketing

Marketing Status
Marketed Since 2015-08-03
Brand memantine
Generic memantine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "33621ba6-ed39-5bf8-e063-6394a90ab7e8", "openfda": {"unii": ["JY0WD0UA60"], "rxcui": ["996561", "996571"], "spl_set_id": ["304a3059-4f7f-4ec4-839d-86492bb5e07b"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "60 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-173-57)  / 1 TABLET in 1 BLISTER PACK (60687-173-11)", "package_ndc": "60687-173-57", "marketing_start_date": "20150803"}], "brand_name": "Memantine", "product_id": "60687-173_33621ba6-ed39-5bf8-e063-6394a90ab7e8", "dosage_form": "TABLET", "pharm_class": ["N-methyl-D-aspartate Receptor Antagonist [EPC]", "NMDA Receptor Antagonists [MoA]"], "product_ndc": "60687-173", "generic_name": "Memantine", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Memantine", "active_ingredients": [{"name": "MEMANTINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA090048", "marketing_category": "ANDA", "marketing_start_date": "20150803", "listing_expiration_date": "20261231"}