United States · FDA National Drug Code directory

Amitriptyline 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: 68788-8363_18c58a61-e63d-43f0-9597-47202ecf8aca
Product NDC: 68788-8363
Form: TABLET, FILM COATED
Composition / generic term: Amitriptyline Hydrochloride
Labeler: Preferred Pharmaceuticals Inc.
Marketing category: ANDA
Marketing start / end (source format): 20230201
Source listing expiry: 20271231

Source-listed ingredients

AMITRIPTYLINE HYDROCHLORIDE — 50 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

30 TABLET, FILM COATED in 1 BOTTLE (68788-8363-3) · 68788-8363-3
60 TABLET, FILM COATED in 1 BOTTLE (68788-8363-6) · 68788-8363-6
28 TABLET, FILM COATED in 1 BOTTLE (68788-8363-8) · 68788-8363-8
90 TABLET, FILM COATED in 1 BOTTLE (68788-8363-9) · 68788-8363-9

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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