Package 60505-6162-5

Brand: memantine

Generic: memantine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60505-6162-5
Digits Only 6050561625
Product NDC 60505-6162
Description

1 BOTTLE in 1 CARTON (60505-6162-5) / 360 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2018-04-30
Brand memantine
Generic memantine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "909dca28-d83f-dbc8-25a0-6f6a40ea2ccc", "openfda": {"unii": ["JY0WD0UA60"], "rxcui": ["996740"], "spl_set_id": ["4076d3ef-d0a9-96c5-1a15-812c1e42929c"], "manufacturer_name": ["Apotex Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (60505-6162-5)  / 360 mL in 1 BOTTLE", "package_ndc": "60505-6162-5", "marketing_start_date": "20180430"}], "brand_name": "MEMANTINE", "product_id": "60505-6162_909dca28-d83f-dbc8-25a0-6f6a40ea2ccc", "dosage_form": "SOLUTION", "pharm_class": ["N-methyl-D-aspartate Receptor Antagonist [EPC]", "NMDA Receptor Antagonists [MoA]"], "product_ndc": "60505-6162", "generic_name": "memantine hydrochloride", "labeler_name": "Apotex Corp.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MEMANTINE", "active_ingredients": [{"name": "MEMANTINE HYDROCHLORIDE", "strength": "2 mg/mL"}], "application_number": "ANDA209955", "marketing_category": "ANDA", "marketing_start_date": "20180430", "listing_expiration_date": "20261231"}