Package 65162-169-06
Brand: memantine hydrochloride
Generic: memantinePackage Facts
Identity
Package NDC
65162-169-06
Digits Only
6516216906
Product NDC
65162-169
Description
60 TABLET, FILM COATED in 1 BOTTLE (65162-169-06)
Marketing
Marketing Status
Brand
memantine hydrochloride
Generic
memantine
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e3662d8d-b6da-40c6-84d4-1b5d467b1eb8", "openfda": {"upc": ["0365162169065"], "unii": ["JY0WD0UA60"], "rxcui": ["996561", "996571"], "spl_set_id": ["f73e0df0-4af4-42f1-bde6-3cccb47ca378"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (65162-169-06)", "package_ndc": "65162-169-06", "marketing_start_date": "20220324"}], "brand_name": "memantine hydrochloride", "product_id": "65162-169_e3662d8d-b6da-40c6-84d4-1b5d467b1eb8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["N-methyl-D-aspartate Receptor Antagonist [EPC]", "NMDA Receptor Antagonists [MoA]"], "product_ndc": "65162-169", "generic_name": "memantine", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "memantine hydrochloride", "active_ingredients": [{"name": "MEMANTINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA090041", "marketing_category": "ANDA", "marketing_start_date": "20220324", "listing_expiration_date": "20261231"}