memantine hydrochloride
Generic: memantine
Labeler: rising pharma holdings, inc.Drug Facts
Product Profile
Brand Name
memantine hydrochloride
Generic Name
memantine
Labeler
rising pharma holdings, inc.
Dosage Form
CAPSULE, EXTENDED RELEASE
Routes
Active Ingredients
memantine hydrochloride 7 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
16571-852
Product ID
16571-852_4ece2bda-d26f-494f-93df-bc53c494caf9
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA206032
Listing Expiration
2026-12-31
Marketing Start
2025-06-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
16571852
Hyphenated Format
16571-852
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 (source: ndc)
Application Number
ANDA206032 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 7 mg/1
Packaging
- 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (16571-852-03)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4ece2bda-d26f-494f-93df-bc53c494caf9", "openfda": {"unii": ["JY0WD0UA60"], "rxcui": ["996594", "996603", "996609", "996615"], "spl_set_id": ["a282fbed-8304-458e-a0e9-5eaccc95339b"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (16571-852-03)", "package_ndc": "16571-852-03", "marketing_start_date": "20250601"}], "brand_name": "Memantine Hydrochloride", "product_id": "16571-852_4ece2bda-d26f-494f-93df-bc53c494caf9", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["N-methyl-D-aspartate Receptor Antagonist [EPC]", "NMDA Receptor Antagonists [MoA]"], "product_ndc": "16571-852", "generic_name": "memantine", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Memantine Hydrochloride", "active_ingredients": [{"name": "MEMANTINE HYDROCHLORIDE", "strength": "7 mg/1"}], "application_number": "ANDA206032", "marketing_category": "ANDA", "marketing_start_date": "20250601", "listing_expiration_date": "20261231"}