memantine hydrochloride
Generic: memantine hydrochloride
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
memantine hydrochloride
Generic Name
memantine hydrochloride
Labeler
remedyrepack inc.
Dosage Form
TABLET
Routes
Active Ingredients
memantine hydrochloride 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-3338
Product ID
70518-3338_36462b8b-8138-11a0-e063-6394a90ad027
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090961
Listing Expiration
2026-12-31
Marketing Start
2022-01-20
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705183338
Hyphenated Format
70518-3338
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
- 60 TABLET in 1 BOTTLE, PLASTIC (70518-3338-1)
- 90 TABLET in 1 BOTTLE, PLASTIC (70518-3338-2)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "36462b8b-8138-11a0-e063-6394a90ad027", "openfda": {"unii": ["JY0WD0UA60"], "rxcui": ["996571"], "spl_set_id": ["cbfd9d95-f50b-45ff-9857-9f1712c45e56"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (70518-3338-1)", "package_ndc": "70518-3338-1", "marketing_start_date": "20250528"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-3338-2)", "package_ndc": "70518-3338-2", "marketing_start_date": "20250528"}], "brand_name": "Memantine Hydrochloride", "product_id": "70518-3338_36462b8b-8138-11a0-e063-6394a90ad027", "dosage_form": "TABLET", "pharm_class": ["N-methyl-D-aspartate Receptor Antagonist [EPC]", "NMDA Receptor Antagonists [MoA]"], "product_ndc": "70518-3338", "generic_name": "Memantine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "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": "20220120", "listing_expiration_date": "20261231"}