United States · FDA National Drug Code directory
Doxepin
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
- 72819-162_0e1f91fa-a035-857e-e063-6394a90a68c9
- Product NDC
- 72819-162
- Form
- TABLET, FILM COATED
- Composition / generic term
- Doxepin
- Labeler
- Archis Pharma LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210801
- Source listing expiry
- 20261231
Source-listed ingredients
- DOXEPIN HYDROCHLORIDE — 6 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE (72819-162-03) · 72819-162-03
- 100 TABLET, FILM COATED in 1 BOTTLE (72819-162-10) · 72819-162-10
- 500 TABLET, FILM COATED in 1 BOTTLE (72819-162-11) · 72819-162-11
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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