donepezil hydrochloride

Generic: donepezil hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name donepezil hydrochloride
Generic Name donepezil hydrochloride
Labeler bryant ranch prepack
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

donepezil hydrochloride 10 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-0900
Product ID 71335-0900_fde8f515-e602-4b77-a4ad-2e829bdaf193
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 713350900
Hyphenated Format 71335-0900

Supplemental Identifiers

RxCUI
997223
UNII
3O2T2PJ89D

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 (71335-0900-1)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71335-0900-2)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71335-0900-3)
source: ndc

Packages (3)

71335-0900-1 30 TABLET, FILM COATED in 1 BOTTLE (71335-0900-1) 71335-0900-2 60 TABLET, FILM COATED in 1 BOTTLE (71335-0900-2) 71335-0900-3 90 TABLET, FILM COATED in 1 BOTTLE (71335-0900-3)

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": "fde8f515-e602-4b77-a4ad-2e829bdaf193", "openfda": {"unii": ["3O2T2PJ89D"], "rxcui": ["997223"], "spl_set_id": ["c26d9bf3-e148-48bb-8f4f-e8c73804b311"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-0900-1)", "package_ndc": "71335-0900-1", "marketing_start_date": "20191001"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-0900-2)", "package_ndc": "71335-0900-2", "marketing_start_date": "20220128"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-0900-3)", "package_ndc": "71335-0900-3", "marketing_start_date": "20180712"}], "brand_name": "donepezil hydrochloride", "product_id": "71335-0900_fde8f515-e602-4b77-a4ad-2e829bdaf193", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "71335-0900", "generic_name": "donepezil hydrochloride", "labeler_name": "Bryant Ranch Prepack", "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"}