memantine hydrochloride

Generic: memantine hydrochloride

Labeler: lupin pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name memantine hydrochloride
Generic Name memantine hydrochloride
Labeler lupin pharmaceuticals, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

memantine hydrochloride 5 mg/1

Manufacturer
Lupin Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68180-229
Product ID 68180-229_392d48fd-7c93-40f3-9ab0-d0f304b7e439
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090051
Listing Expiration 2026-12-31
Marketing Start 2015-07-13

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 68180229
Hyphenated Format 68180-229

Supplemental Identifiers

RxCUI
996561 996571
UPC
0368180230076 0368180229070
UNII
JY0WD0UA60

Packaging Origin

Original Packager
true

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 ANDA090051 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 60 TABLET, FILM COATED in 1 BOTTLE (68180-229-07)
source: ndc

Packages (1)

68180-229-07 60 TABLET, FILM COATED in 1 BOTTLE (68180-229-07)

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": "392d48fd-7c93-40f3-9ab0-d0f304b7e439", "openfda": {"upc": ["0368180230076", "0368180229070"], "unii": ["JY0WD0UA60"], "rxcui": ["996561", "996571"], "spl_set_id": ["1b4a0162-9cb4-4ba6-8c02-95c2955734ae"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68180-229-07)", "package_ndc": "68180-229-07", "marketing_start_date": "20150713"}], "brand_name": "Memantine hydrochloride", "product_id": "68180-229_392d48fd-7c93-40f3-9ab0-d0f304b7e439", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["N-methyl-D-aspartate Receptor Antagonist [EPC]", "NMDA Receptor Antagonists [MoA]"], "product_ndc": "68180-229", "generic_name": "Memantine hydrochloride", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Memantine hydrochloride", "active_ingredients": [{"name": "MEMANTINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA090051", "marketing_category": "ANDA", "marketing_start_date": "20150713", "listing_expiration_date": "20261231"}