Package 0832-1112-60

Brand: memantine hydrochloride

Generic: memantine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0832-1112-60
Digits Only 0832111260
Product NDC 0832-1112
Description

60 TABLET, FILM COATED in 1 BOTTLE (0832-1112-60)

Marketing

Marketing Status
Discontinued 2028-01-31
Brand memantine hydrochloride
Generic memantine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "45af280b-1724-c805-e063-6294a90a76ee", "openfda": {"upc": ["0308321113608"], "unii": ["JY0WD0UA60"], "rxcui": ["996561", "996571"], "spl_set_id": ["6e0ade9e-b721-4701-bcb7-de464e19e707"], "manufacturer_name": ["Upsher-Smith Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (0832-1112-60)", "package_ndc": "0832-1112-60", "marketing_end_date": "20280131", "marketing_start_date": "20150731"}], "brand_name": "Memantine Hydrochloride", "product_id": "0832-1112_45af280b-1724-c805-e063-6294a90a76ee", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["N-methyl-D-aspartate Receptor Antagonist [EPC]", "NMDA Receptor Antagonists [MoA]"], "product_ndc": "0832-1112", "generic_name": "Memantine Hydrochloride", "labeler_name": "Upsher-Smith Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Memantine Hydrochloride", "active_ingredients": [{"name": "MEMANTINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA090043", "marketing_category": "ANDA", "marketing_end_date": "20280131", "marketing_start_date": "20150731"}