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
Routes
ORAL
Active Ingredients

donepezil hydrochloride 10 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-2436
Product ID 71335-2436_255eaadf-bf5d-45d2-ac99-906d14d655c9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078662
Listing Expiration 2026-12-31
Marketing Start 2021-06-29

Pharmacologic Class

Classes
cholinesterase inhibitor [epc] cholinesterase inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713352436
Hyphenated Format 71335-2436

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 ANDA078662 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-2436-1)
  • 60 TABLET in 1 BOTTLE (71335-2436-2)
  • 90 TABLET in 1 BOTTLE (71335-2436-3)
source: ndc

Packages (3)

71335-2436-1 30 TABLET in 1 BOTTLE (71335-2436-1) 71335-2436-2 60 TABLET in 1 BOTTLE (71335-2436-2) 71335-2436-3 90 TABLET in 1 BOTTLE (71335-2436-3)

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": "255eaadf-bf5d-45d2-ac99-906d14d655c9", "openfda": {"unii": ["3O2T2PJ89D"], "rxcui": ["997223"], "spl_set_id": ["7db089de-0344-4246-81b7-7c88a2a18402"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2436-1)", "package_ndc": "71335-2436-1", "marketing_start_date": "20240715"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-2436-2)", "package_ndc": "71335-2436-2", "marketing_start_date": "20240715"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2436-3)", "package_ndc": "71335-2436-3", "marketing_start_date": "20240715"}], "brand_name": "Donepezil Hydrochloride", "product_id": "71335-2436_255eaadf-bf5d-45d2-ac99-906d14d655c9", "dosage_form": "TABLET", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "71335-2436", "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": "ANDA078662", "marketing_category": "ANDA", "marketing_start_date": "20210629", "listing_expiration_date": "20261231"}