NDC 71335-2769 – Amitriptyline Hydrochloride

Amitriptyline Hydrochloride 25 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC71335-2769

Product details

Brand name
Amitriptyline Hydrochloride
Generic name
Amitriptyline Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA212654
Marketed since
May 20, 2024
Listing expires
December 31, 2026
Pharmacologic class
Tricyclic Antidepressant

Active ingredients

Uses, dosage, side effects and warnings for Amitriptyline Hydrochloride →

Package NDC codes (10)

Package NDCDescriptionSince
71335-2769-0120 TABLET, COATED in 1 BOTTLE (71335-2769-0)Oct 3, 2025
71335-2769-120 TABLET, COATED in 1 BOTTLE (71335-2769-1)Oct 3, 2025
71335-2769-230 TABLET, COATED in 1 BOTTLE (71335-2769-2)Oct 3, 2025
71335-2769-3100 TABLET, COATED in 1 BOTTLE (71335-2769-3)Oct 3, 2025
71335-2769-460 TABLET, COATED in 1 BOTTLE (71335-2769-4)Oct 3, 2025
71335-2769-550 TABLET, COATED in 1 BOTTLE (71335-2769-5)Oct 3, 2025
71335-2769-690 TABLET, COATED in 1 BOTTLE (71335-2769-6)Oct 3, 2025
71335-2769-745 TABLET, COATED in 1 BOTTLE (71335-2769-7)Oct 3, 2025
71335-2769-828 TABLET, COATED in 1 BOTTLE (71335-2769-8)Oct 3, 2025
71335-2769-956 TABLET, COATED in 1 BOTTLE (71335-2769-9)Oct 3, 2025

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