memantine hydrochloride
Generic: memantine hydrochloride
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
memantine hydrochloride
Generic Name
memantine hydrochloride
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
memantine hydrochloride 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
63629-2512
Product ID
63629-2512_f05f0498-106d-45f5-9509-dcbd3a25d062
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090961
Listing Expiration
2026-12-31
Marketing Start
2019-02-28
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
636292512
Hyphenated Format
63629-2512
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
- 10 mg/1
Packaging
- 60 TABLET in 1 BOTTLE (63629-2512-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f05f0498-106d-45f5-9509-dcbd3a25d062", "openfda": {"unii": ["JY0WD0UA60"], "rxcui": ["996561"], "spl_set_id": ["c8f96b24-de66-4a17-b798-42b42a25e84c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (63629-2512-1)", "package_ndc": "63629-2512-1", "marketing_start_date": "20210518"}], "brand_name": "Memantine Hydrochloride", "product_id": "63629-2512_f05f0498-106d-45f5-9509-dcbd3a25d062", "dosage_form": "TABLET", "pharm_class": ["N-methyl-D-aspartate Receptor Antagonist [EPC]", "NMDA Receptor Antagonists [MoA]"], "product_ndc": "63629-2512", "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": "ANDA090961", "marketing_category": "ANDA", "marketing_start_date": "20190228", "listing_expiration_date": "20261231"}