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
48433-037_4c4c90ec-fb2d-e45d-e063-6294a90a419a
Product NDC
48433-037
Form
CAPSULE
Composition / generic term
doxepin hydrochloride
Labeler
Safecor Health, LLC
Marketing category
ANDA
Marketing start / end (source format)
20260223
Source listing expiry
20271231

Source-listed ingredients

  • DOXEPIN HYDROCHLORIDE — 50 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 BLISTER PACK in 1 CARTON (48433-037-20) / 1 CAPSULE in 1 BLISTER PACK (48433-037-01) · 48433-037-20

Source and coverage

Open FDA National Drug Code directory

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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Doxepin Hydrochloride — United States | Molindra Medicines