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
- 71335-2772_08c0027e-4168-43c2-a7d9-f6555bf250ef
- Product NDC
- 71335-2772
- Form
- CAPSULE
- Composition / generic term
- Nortriptyline Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20231117
- Source listing expiry
- 20261231
Source-listed ingredients
- NORTRIPTYLINE HYDROCHLORIDE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 CAPSULE in 1 BOTTLE, PLASTIC (71335-2772-1) · 71335-2772-1
- 60 CAPSULE in 1 BOTTLE, PLASTIC (71335-2772-2) · 71335-2772-2
- 90 CAPSULE in 1 BOTTLE, PLASTIC (71335-2772-3) · 71335-2772-3
- 100 CAPSULE in 1 BOTTLE, PLASTIC (71335-2772-4) · 71335-2772-4
- 120 CAPSULE in 1 BOTTLE, PLASTIC (71335-2772-5) · 71335-2772-5
- 15 CAPSULE in 1 BOTTLE, PLASTIC (71335-2772-6) · 71335-2772-6
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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