memantine hydrochloride
Generic: memantine hydrochloride
Labeler: directrxDrug Facts
Product Profile
Brand Name
memantine hydrochloride
Generic Name
memantine hydrochloride
Labeler
directrx
Dosage Form
TABLET
Routes
Active Ingredients
memantine hydrochloride 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72189-294
Product ID
72189-294_4c5d26cb-a6bf-015e-e063-6294a90aa662
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090961
Listing Expiration
2027-12-31
Marketing Start
2021-11-11
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72189294
Hyphenated Format
72189-294
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
ANDA090961 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (72189-294-30)
- 60 TABLET in 1 BOTTLE (72189-294-60)
- 90 TABLET in 1 BOTTLE (72189-294-90)
Packages (3)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4c5d26cb-a6bf-015e-e063-6294a90aa662", "openfda": {"unii": ["JY0WD0UA60"], "rxcui": ["996571"], "spl_set_id": ["d0839a2d-35f1-1f14-e053-2995a90ad549"], "manufacturer_name": ["DirectRx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-294-30)", "package_ndc": "72189-294-30", "marketing_start_date": "20211111"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (72189-294-60)", "package_ndc": "72189-294-60", "marketing_start_date": "20211111"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-294-90)", "package_ndc": "72189-294-90", "marketing_start_date": "20211111"}], "brand_name": "MEMANTINE HYDROCHLORIDE", "product_id": "72189-294_4c5d26cb-a6bf-015e-e063-6294a90aa662", "dosage_form": "TABLET", "pharm_class": ["N-methyl-D-aspartate Receptor Antagonist [EPC]", "NMDA Receptor Antagonists [MoA]"], "product_ndc": "72189-294", "generic_name": "MEMANTINE HYDROCHLORIDE", "labeler_name": "DirectRx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MEMANTINE HYDROCHLORIDE", "active_ingredients": [{"name": "MEMANTINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA090961", "marketing_category": "ANDA", "marketing_start_date": "20211111", "listing_expiration_date": "20271231"}