memantine hydrochloride
Generic: memantine hydrochloride
Labeler: upsher-smith laboratories, llcDrug Facts
Product Profile
Brand Name
memantine hydrochloride
Generic Name
memantine hydrochloride
Labeler
upsher-smith laboratories, llc
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
memantine hydrochloride 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0832-1112
Product ID
0832-1112_45af280b-1724-c805-e063-6294a90a76ee
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090043
Marketing Start
2015-07-31
Marketing End
2028-01-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
08321112
Hyphenated Format
0832-1112
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
memantine hydrochloride (source: ndc)
Generic Name
memantine hydrochloride (source: ndc)
Application Number
ANDA090043 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 60 TABLET, FILM COATED in 1 BOTTLE (0832-1112-60)
Packages (1)
Ingredients (1)
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"}