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
- 27241-171_fa508191-83f3-4352-8389-a7e3cb80cb1c
- Product NDC
- 27241-171
- Form
- CAPSULE
- Composition / generic term
- Doxepin hydrochloride
- Labeler
- Ajanta Pharma USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20191220
- Source listing expiry
- 20271231
Source-listed ingredients
- DOXEPIN HYDROCHLORIDE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE in 1 BOTTLE (27241-171-01) · 27241-171-01
- 1000 CAPSULE in 1 BOTTLE (27241-171-10) · 27241-171-10
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 →