United States · FDA National Drug Code directory

Donepezil Hydrochloride

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference: 71335-2093_280c4887-57c3-4d43-afca-98e64de44219
Product NDC: 71335-2093
Form: TABLET, FILM COATED
Composition / generic term: Donepezil Hydrochloride
Labeler: Bryant Ranch Prepack
Marketing category: ANDA
Marketing start / end (source format): 20110531
Source listing expiry: 20261231

Source-listed ingredients

DONEPEZIL HYDROCHLORIDE — 5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

90 TABLET, FILM COATED in 1 BOTTLE (71335-2093-1) · 71335-2093-1
30 TABLET, FILM COATED in 1 BOTTLE (71335-2093-2) · 71335-2093-2
60 TABLET, FILM COATED in 1 BOTTLE (71335-2093-3) · 71335-2093-3

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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