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
- 65862-326_3c956648-d46c-41e2-a2d9-8560846a7a32
- Product NDC
- 65862-326
- Form
- TABLET, FILM COATED
- Composition / generic term
- Donepezil Hydrochloride
- Labeler
- Aurobindo Pharma Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20110531
- Source listing expiry
- 20261231
Source-listed ingredients
- DONEPEZIL HYDROCHLORIDE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (65862-326-01) · 65862-326-01
- 500 TABLET, FILM COATED in 1 BOTTLE (65862-326-05) · 65862-326-05
- 10 BLISTER PACK in 1 CARTON (65862-326-14) / 14 TABLET, FILM COATED in 1 BLISTER PACK · 65862-326-14
- 30 TABLET, FILM COATED in 1 BOTTLE (65862-326-30) · 65862-326-30
- 90 TABLET, FILM COATED in 1 BOTTLE (65862-326-90) · 65862-326-90
- 1000 TABLET, FILM COATED in 1 BOTTLE (65862-326-99) · 65862-326-99
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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