NDC 71335-2802 – Amitriptyline Hydrochloride

Amitriptyline Hydrochloride 50 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC71335-2802

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 (8)

Package NDCDescriptionSince
71335-2802-1100 TABLET, COATED in 1 BOTTLE (71335-2802-1)Oct 3, 2025
71335-2802-230 TABLET, COATED in 1 BOTTLE (71335-2802-2)Oct 3, 2025
71335-2802-360 TABLET, COATED in 1 BOTTLE (71335-2802-3)Oct 3, 2025
71335-2802-490 TABLET, COATED in 1 BOTTLE (71335-2802-4)Oct 3, 2025
71335-2802-520 TABLET, COATED in 1 BOTTLE (71335-2802-5)Oct 3, 2025
71335-2802-628 TABLET, COATED in 1 BOTTLE (71335-2802-6)Oct 3, 2025
71335-2802-756 TABLET, COATED in 1 BOTTLE (71335-2802-7)Oct 3, 2025
71335-2802-8180 TABLET, COATED in 1 BOTTLE (71335-2802-8)Oct 3, 2025

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