memantine hydrochloride
Generic: memantine hydrochloride
Labeler: actavis pharma, inc.Drug Facts
Product Profile
Brand Name
memantine hydrochloride
Generic Name
memantine hydrochloride
Labeler
actavis pharma, inc.
Dosage Form
KIT
Routes
Manufacturer
Identifiers & Regulatory
Product NDC
0591-3900
Product ID
0591-3900_985e1190-b8a0-4775-9a20-ad1924b14fb2
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA AUTHORIZED GENERIC
Application Number
NDA021487
Marketing Start
2015-04-01
Marketing End
2028-08-31
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
05913900
Hyphenated Format
0591-3900
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
NDA021487 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg
- 10 mg
- 10 unit
Packaging
- 1 BLISTER PACK in 1 CARTON (0591-3900-87) / 1 KIT in 1 BLISTER PACK
Packages (1)
Ingredients (0)
No ingredient records.
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "985e1190-b8a0-4775-9a20-ad1924b14fb2", "openfda": {"unii": ["JY0WD0UA60"], "rxcui": ["996561", "996571", "996572"], "spl_set_id": ["72973b46-f307-4a9e-8fb1-ad2cbccfd736"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (0591-3900-87) / 1 KIT in 1 BLISTER PACK", "package_ndc": "0591-3900-87", "marketing_end_date": "20280831", "marketing_start_date": "20150401"}], "brand_name": "memantine hydrochloride", "product_id": "0591-3900_985e1190-b8a0-4775-9a20-ad1924b14fb2", "dosage_form": "KIT", "product_ndc": "0591-3900", "generic_name": "memantine hydrochloride", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "memantine hydrochloride", "application_number": "NDA021487", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_end_date": "20280831", "marketing_start_date": "20150401"}