memantine hydrochloride

Generic: memantine hydrochloride

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name memantine hydrochloride
Generic Name memantine hydrochloride
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

memantine hydrochloride 5 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-5926
Product ID 50090-5926_99e7c450-2c83-487e-a326-76c1653723b8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200022
Listing Expiration 2026-12-31
Marketing Start 2015-11-01

Pharmacologic Class

Classes
n-methyl-d-aspartate receptor antagonist [epc] nmda receptor antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500905926
Hyphenated Format 50090-5926

Supplemental Identifiers

RxCUI
996571
UNII
JY0WD0UA60

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 ANDA200022 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 60 TABLET, FILM COATED in 1 BOTTLE (50090-5926-0)
  • 90 TABLET, FILM COATED in 1 BOTTLE (50090-5926-1)
source: ndc

Packages (2)

50090-5926-0 60 TABLET, FILM COATED in 1 BOTTLE (50090-5926-0) 50090-5926-1 90 TABLET, FILM COATED in 1 BOTTLE (50090-5926-1)

Ingredients (1)

memantine hydrochloride (5 mg/1)

Linked Drug Pages (1)

Memantine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "99e7c450-2c83-487e-a326-76c1653723b8", "openfda": {"unii": ["JY0WD0UA60"], "rxcui": ["996571"], "spl_set_id": ["2fdf0b2b-0337-472d-83ec-075c17c9b0d0"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (50090-5926-0)", "package_ndc": "50090-5926-0", "marketing_start_date": "20220301"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-5926-1)", "package_ndc": "50090-5926-1", "marketing_start_date": "20220702"}], "brand_name": "Memantine Hydrochloride", "product_id": "50090-5926_99e7c450-2c83-487e-a326-76c1653723b8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["N-methyl-D-aspartate Receptor Antagonist [EPC]", "NMDA Receptor Antagonists [MoA]"], "product_ndc": "50090-5926", "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": "5 mg/1"}], "application_number": "ANDA200022", "marketing_category": "ANDA", "marketing_start_date": "20151101", "listing_expiration_date": "20261231"}