memantine hydrochloride

Generic: memantine hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name memantine hydrochloride
Generic Name memantine hydrochloride
Labeler bryant ranch prepack
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

memantine hydrochloride 10 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1908
Product ID 71335-1908_417d1056-9d1c-47c4-a065-ca8bd6397982
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090058
Listing Expiration 2026-12-31
Marketing Start 2015-07-11

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 713351908
Hyphenated Format 71335-1908

Supplemental Identifiers

RxCUI
996561
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 ANDA090058 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (71335-1908-1)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71335-1908-2)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71335-1908-3)
  • 180 TABLET, FILM COATED in 1 BOTTLE (71335-1908-4)
source: ndc

Packages (4)

Ingredients (1)

memantine hydrochloride (10 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "417d1056-9d1c-47c4-a065-ca8bd6397982", "openfda": {"unii": ["JY0WD0UA60"], "rxcui": ["996561"], "spl_set_id": ["2ac7d23c-5f9f-4ffc-ae01-d7099a8a7929"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-1908-1)", "package_ndc": "71335-1908-1", "marketing_start_date": "20210715"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-1908-2)", "package_ndc": "71335-1908-2", "marketing_start_date": "20210715"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-1908-3)", "package_ndc": "71335-1908-3", "marketing_start_date": "20210715"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (71335-1908-4)", "package_ndc": "71335-1908-4", "marketing_start_date": "20210715"}], "brand_name": "Memantine Hydrochloride", "product_id": "71335-1908_417d1056-9d1c-47c4-a065-ca8bd6397982", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["N-methyl-D-aspartate Receptor Antagonist [EPC]", "NMDA Receptor Antagonists [MoA]"], "product_ndc": "71335-1908", "generic_name": "Memantine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Memantine Hydrochloride", "active_ingredients": [{"name": "MEMANTINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA090058", "marketing_category": "ANDA", "marketing_start_date": "20150711", "listing_expiration_date": "20261231"}