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
- 71093-128_a4736add-da84-411f-8e6f-9de67bf467f8
- Product NDC
- 71093-128
- Form
- TABLET
- Composition / generic term
- Donepezil Hydrochloride
- Labeler
- ACI Healthcare USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210629
- Source listing expiry
- 20261231
Source-listed ingredients
- DONEPEZIL HYDROCHLORIDE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (71093-128-01) · 71093-128-01
- 90 TABLET in 1 BOTTLE (71093-128-03) · 71093-128-03
- 500 TABLET in 1 BOTTLE (71093-128-05) · 71093-128-05
- 1000 TABLET in 1 BOTTLE (71093-128-06) · 71093-128-06
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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