United States · FDA National Drug Code directory
Nortriptyline 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
- 51672-4004_56a6d4f3-e026-2d59-e063-6394a90a45be
- Product NDC
- 51672-4004
- Form
- CAPSULE
- Composition / generic term
- Nortriptyline Hydrochloride
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20000508
- Source listing expiry
- 20271231
Source-listed ingredients
- NORTRIPTYLINE HYDROCHLORIDE — 75 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE in 1 BOTTLE (51672-4004-1) · 51672-4004-1
- 500 CAPSULE in 1 BOTTLE (51672-4004-2) · 51672-4004-2
- 90 CAPSULE in 1 BOTTLE (51672-4004-5) · 51672-4004-5
- 30 CAPSULE in 1 BOTTLE (51672-4004-6) · 51672-4004-6
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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