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
- 82804-302_1e32f284-a5b2-4ebf-9d9e-0e9a40b46ade
- Product NDC
- 82804-302
- Form
- CAPSULE
- Composition / generic term
- Nortriptyline Hydrochloride
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20231117
- Source listing expiry
- 20271231
Source-listed ingredients
- NORTRIPTYLINE HYDROCHLORIDE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 90 CAPSULE in 1 BOTTLE, PLASTIC (82804-302-90) · 82804-302-90
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 →