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
- 29300-251_88d3f867-45f4-42fb-93f8-235c2f594760
- Product NDC
- 29300-251
- Form
- TABLET, ORALLY DISINTEGRATING
- Composition / generic term
- donepezil hydrochloride
- Labeler
- Unichem Pharmaceuticals (USA), Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20161110
- Source listing expiry
- 20261231
Source-listed ingredients
- DONEPEZIL HYDROCHLORIDE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 3 BLISTER PACK in 1 CARTON (29300-251-87) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (29300-251-11) · 29300-251-87
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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