memantine hydrochloride

Generic: memantine hydrochloride

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

Drug Facts

Product Profile

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

memantine hydrochloride 5 mg/1

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-807
Product ID 31722-807_eabf0e61-425e-9c9f-e053-2a95a90ade8e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204389
Listing Expiration 2026-12-31
Marketing Start 2022-09-26

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 31722807
Hyphenated Format 31722-807

Supplemental Identifiers

RxCUI
996561 996571
UPC
0331722807609 0331722808606
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 ANDA204389 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 200 TABLET in 1 BOTTLE (31722-807-02)
  • 10 BLISTER PACK in 1 CARTON (31722-807-32) / 10 TABLET in 1 BLISTER PACK
  • 60 TABLET in 1 BOTTLE (31722-807-60)
source: ndc

Packages (3)

31722-807-02 200 TABLET in 1 BOTTLE (31722-807-02) 31722-807-32 10 BLISTER PACK in 1 CARTON (31722-807-32) / 10 TABLET in 1 BLISTER PACK 31722-807-60 60 TABLET in 1 BOTTLE (31722-807-60)

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": "eabf0e61-425e-9c9f-e053-2a95a90ade8e", "openfda": {"upc": ["0331722807609", "0331722808606"], "unii": ["JY0WD0UA60"], "rxcui": ["996561", "996571"], "spl_set_id": ["910827aa-5320-446c-8f66-3f17c0ee36d9"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 TABLET in 1 BOTTLE (31722-807-02)", "package_ndc": "31722-807-02", "marketing_start_date": "20220926"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (31722-807-32)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "31722-807-32", "marketing_start_date": "20220926"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (31722-807-60)", "package_ndc": "31722-807-60", "marketing_start_date": "20220926"}], "brand_name": "memantine hydrochloride", "product_id": "31722-807_eabf0e61-425e-9c9f-e053-2a95a90ade8e", "dosage_form": "TABLET", "pharm_class": ["N-methyl-D-aspartate Receptor Antagonist [EPC]", "NMDA Receptor Antagonists [MoA]"], "product_ndc": "31722-807", "generic_name": "memantine hydrochloride", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "memantine hydrochloride", "active_ingredients": [{"name": "MEMANTINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA204389", "marketing_category": "ANDA", "marketing_start_date": "20220926", "listing_expiration_date": "20261231"}