NDC 71335-9668 – Amitriptyline Hydrochloride

Amitriptyline Hydrochloride 100 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-9668

Product details

Brand name
Amitriptyline Hydrochloride
Generic name
Amitriptyline Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA214548
Marketed since
May 26, 2021
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
71335-9668-130 TABLET, FILM COATED in 1 BOTTLE (71335-9668-1)Mar 27, 2023
71335-9668-260 TABLET, FILM COATED in 1 BOTTLE (71335-9668-2)Mar 27, 2023
71335-9668-390 TABLET, FILM COATED in 1 BOTTLE (71335-9668-3)Mar 27, 2023
71335-9668-4180 TABLET, FILM COATED in 1 BOTTLE (71335-9668-4)Mar 27, 2023
71335-9668-528 TABLET, FILM COATED in 1 BOTTLE (71335-9668-5)Mar 27, 2023
71335-9668-6120 TABLET, FILM COATED in 1 BOTTLE (71335-9668-6)Mar 27, 2023
71335-9668-718 TABLET, FILM COATED in 1 BOTTLE (71335-9668-7)Mar 27, 2023
71335-9668-88 TABLET, FILM COATED in 1 BOTTLE (71335-9668-8)Mar 27, 2023

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