memantine hydrochloride
Generic: memantine hydrochloride
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
memantine hydrochloride
Generic Name
memantine hydrochloride
Labeler
a-s medication solutions
Dosage Form
TABLET
Routes
Active Ingredients
memantine hydrochloride 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-6400
Product ID
50090-6400_0f1a6f0c-50ec-4e4b-a804-5385a2fd2e40
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA206528
Listing Expiration
2026-12-31
Marketing Start
2015-08-27
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500906400
Hyphenated Format
50090-6400
Supplemental Identifiers
RxCUI
UNII
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
ANDA206528 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 90 TABLET in 1 BOTTLE (50090-6400-0)
- 60 TABLET in 1 BOTTLE (50090-6400-1)
- 180 TABLET in 1 BOTTLE (50090-6400-2)
Packages (3)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0f1a6f0c-50ec-4e4b-a804-5385a2fd2e40", "openfda": {"unii": ["JY0WD0UA60"], "rxcui": ["996561"], "spl_set_id": ["d1c2ec99-7183-46e3-a96e-4f23e20b8b06"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-6400-0)", "package_ndc": "50090-6400-0", "marketing_start_date": "20230316"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-6400-1)", "package_ndc": "50090-6400-1", "marketing_start_date": "20230316"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (50090-6400-2)", "package_ndc": "50090-6400-2", "marketing_start_date": "20230316"}], "brand_name": "Memantine Hydrochloride", "product_id": "50090-6400_0f1a6f0c-50ec-4e4b-a804-5385a2fd2e40", "dosage_form": "TABLET", "pharm_class": ["N-methyl-D-aspartate Receptor Antagonist [EPC]", "NMDA Receptor Antagonists [MoA]"], "product_ndc": "50090-6400", "generic_name": "Memantine Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Memantine Hydrochloride", "active_ingredients": [{"name": "MEMANTINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA206528", "marketing_category": "ANDA", "marketing_start_date": "20150827", "listing_expiration_date": "20261231"}