memantine hydrochloride

Generic: memantine hydrochloride

Labeler: ajanta pharma usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name memantine hydrochloride
Generic Name memantine hydrochloride
Labeler ajanta pharma usa inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

memantine hydrochloride 10 mg/1

Manufacturer
Ajanta Pharma USA Inc.

Identifiers & Regulatory

Product NDC 27241-071
Product ID 27241-071_078be4f6-c883-4178-be61-834fb9d5e4f5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206528
Listing Expiration 2026-12-31
Marketing Start 2015-08-27

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 27241071
Hyphenated Format 27241-071

Supplemental Identifiers

RxCUI
996561 996571
UPC
0327241070068 0327241071065
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 ANDA206528 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 500 TABLET in 1 BOTTLE (27241-071-05)
  • 60 TABLET in 1 BOTTLE (27241-071-06)
source: ndc

Packages (2)

27241-071-05 500 TABLET in 1 BOTTLE (27241-071-05) 27241-071-06 60 TABLET in 1 BOTTLE (27241-071-06)

Ingredients (1)

memantine hydrochloride (10 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": "078be4f6-c883-4178-be61-834fb9d5e4f5", "openfda": {"upc": ["0327241070068", "0327241071065"], "unii": ["JY0WD0UA60"], "rxcui": ["996561", "996571"], "spl_set_id": ["292671f2-f221-4a3d-a110-a266a9527e04"], "manufacturer_name": ["Ajanta Pharma USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (27241-071-05)", "package_ndc": "27241-071-05", "marketing_start_date": "20150827"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (27241-071-06)", "package_ndc": "27241-071-06", "marketing_start_date": "20150827"}], "brand_name": "Memantine Hydrochloride", "product_id": "27241-071_078be4f6-c883-4178-be61-834fb9d5e4f5", "dosage_form": "TABLET", "pharm_class": ["N-methyl-D-aspartate Receptor Antagonist [EPC]", "NMDA Receptor Antagonists [MoA]"], "product_ndc": "27241-071", "generic_name": "Memantine Hydrochloride", "labeler_name": "Ajanta Pharma USA Inc.", "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"}