United States · FDA National Drug Code directory
Doxepin 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
- 81469-415_55da757c-42d2-4963-b06f-def9f18a423f
- Product NDC
- 81469-415
- Form
- CAPSULE
- Composition / generic term
- doxepin hydrochloride
- Labeler
- First Nation Group, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230111
- Source listing expiry
- 20261231
Source-listed ingredients
- DOXEPIN HYDROCHLORIDE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE in 1 BOTTLE (81469-415-01) · 81469-415-01
- 500 CAPSULE in 1 BOTTLE (81469-415-05) · 81469-415-05
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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