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
64980-597_2877d1f2-a036-4577-926d-b09828350ea1
Product NDC
64980-597
Form
CAPSULE
Composition / generic term
Doxepin hydrochloride
Labeler
Rising Pharma Holdings, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20231225
Source listing expiry
20261231

Source-listed ingredients

  • DOXEPIN HYDROCHLORIDE — 75 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 CAPSULE in 1 BOTTLE (64980-597-01) · 64980-597-01

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.

Browse United States records →