donepezil hydrochloride

Generic: donepezil hydrochloride

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

donepezil hydrochloride 5 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-031
Product ID 72189-031_2c4e974d-41bb-49ca-e063-6394a90ae3a0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200292
Listing Expiration 2026-12-31
Marketing Start 2019-10-01

Pharmacologic Class

Classes
cholinesterase inhibitor [epc] cholinesterase inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189031
Hyphenated Format 72189-031

Supplemental Identifiers

RxCUI
997229
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
  • 5 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (72189-031-30)
source: ndc

Packages (1)

72189-031-30 30 TABLET, FILM COATED in 1 BOTTLE (72189-031-30)

Ingredients (1)

donepezil hydrochloride (5 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": "2c4e974d-41bb-49ca-e063-6394a90ae3a0", "openfda": {"unii": ["3O2T2PJ89D"], "rxcui": ["997229"], "spl_set_id": ["93dddf28-094b-dd8c-e053-2995a90a63e9"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-031-30)", "package_ndc": "72189-031-30", "marketing_start_date": "20191001"}], "brand_name": "DONEPEZIL HYDROCHLORIDE", "product_id": "72189-031_2c4e974d-41bb-49ca-e063-6394a90ae3a0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "72189-031", "generic_name": "DONEPEZIL HYDROCHLORIDE", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DONEPEZIL HYDROCHLORIDE", "active_ingredients": [{"name": "DONEPEZIL HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA200292", "marketing_category": "ANDA", "marketing_start_date": "20191001", "listing_expiration_date": "20261231"}