donepezil hydrochloride

Generic: donepezil hydrochloride

Labeler: solco healthcare us, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name donepezil hydrochloride
Generic Name donepezil hydrochloride
Labeler solco healthcare us, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

donepezil hydrochloride 10 mg/1

Manufacturer
Solco Healthcare US, LLC

Identifiers & Regulatory

Product NDC 43547-276
Product ID 43547-276_dcfd9a94-e1bc-4b53-ae6f-0200ee714917
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200292
Listing Expiration 2026-12-31
Marketing Start 2011-11-01

Pharmacologic Class

Classes
cholinesterase inhibitor [epc] cholinesterase inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 43547276
Hyphenated Format 43547-276

Supplemental Identifiers

RxCUI
997223 997229
UPC
0343547276034 0343547275037
UNII
3O2T2PJ89D

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 donepezil hydrochloride (source: ndc)
Generic Name donepezil hydrochloride (source: ndc)
Application Number ANDA200292 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-276-03)
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-276-09)
  • 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-276-11)
source: ndc

Packages (3)

43547-276-03 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-276-03) 43547-276-09 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-276-09) 43547-276-11 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-276-11)

Ingredients (1)

donepezil hydrochloride (10 mg/1)

Linked Drug Pages (1)

donepezil hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "dcfd9a94-e1bc-4b53-ae6f-0200ee714917", "openfda": {"upc": ["0343547276034", "0343547275037"], "unii": ["3O2T2PJ89D"], "rxcui": ["997223", "997229"], "spl_set_id": ["042a59ea-131a-4806-b0f4-2f791d4414e2"], "manufacturer_name": ["Solco Healthcare US, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-276-03)", "package_ndc": "43547-276-03", "marketing_start_date": "20111101"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-276-09)", "package_ndc": "43547-276-09", "marketing_start_date": "20111101"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-276-11)", "package_ndc": "43547-276-11", "marketing_start_date": "20111101"}], "brand_name": "donepezil hydrochloride", "product_id": "43547-276_dcfd9a94-e1bc-4b53-ae6f-0200ee714917", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "43547-276", "generic_name": "donepezil hydrochloride", "labeler_name": "Solco Healthcare US, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "donepezil hydrochloride", "active_ingredients": [{"name": "DONEPEZIL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA200292", "marketing_category": "ANDA", "marketing_start_date": "20111101", "listing_expiration_date": "20261231"}