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
- 70771-1614_b2965133-3b71-4cdb-8676-235882e57beb
- Product NDC
- 70771-1614
- Form
- CAPSULE
- Composition / generic term
- Nortriptyline Hydrochloride
- Labeler
- Zydus Lifesciences Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220210
- Source listing expiry
- 20261231
Source-listed ingredients
- NORTRIPTYLINE HYDROCHLORIDE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE in 1 BOTTLE (70771-1614-1) · 70771-1614-1
- 30 CAPSULE in 1 BOTTLE (70771-1614-3) · 70771-1614-3
- 500 CAPSULE in 1 BOTTLE (70771-1614-5) · 70771-1614-5
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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