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
Routes
ORAL
Active Ingredients

memantine hydrochloride 5 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1732
Product ID 71335-1732_216899e3-38c6-4ac6-9ffc-ec5264ef4246
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090961
Listing Expiration 2026-12-31
Marketing Start 2019-02-28

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 713351732
Hyphenated Format 71335-1732

Supplemental Identifiers

RxCUI
996571
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 ANDA090961 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-1732-1)
  • 60 TABLET in 1 BOTTLE (71335-1732-2)
source: ndc

Packages (2)

Ingredients (1)

memantine hydrochloride (5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "216899e3-38c6-4ac6-9ffc-ec5264ef4246", "openfda": {"unii": ["JY0WD0UA60"], "rxcui": ["996571"], "spl_set_id": ["9cfddd01-6e1d-4ee0-9310-3fb371724e3d"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1732-1)", "package_ndc": "71335-1732-1", "marketing_start_date": "20201111"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-1732-2)", "package_ndc": "71335-1732-2", "marketing_start_date": "20201111"}], "brand_name": "Memantine Hydrochloride", "product_id": "71335-1732_216899e3-38c6-4ac6-9ffc-ec5264ef4246", "dosage_form": "TABLET", "pharm_class": ["N-methyl-D-aspartate Receptor Antagonist [EPC]", "NMDA Receptor Antagonists [MoA]"], "product_ndc": "71335-1732", "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": "5 mg/1"}], "application_number": "ANDA090961", "marketing_category": "ANDA", "marketing_start_date": "20190228", "listing_expiration_date": "20261231"}