NDC 71335-1256 – Amitriptyline Hydrochloride

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

Human Prescription Drug

Product NDC71335-1256

Product details

Brand name
Amitriptyline Hydrochloride
Generic name
Amitriptyline Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA089399
Marketed since
July 14, 1987
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
71335-1256-1100 TABLET, FILM COATED in 1 BOTTLE (71335-1256-1)Feb 9, 2022
71335-1256-230 TABLET, FILM COATED in 1 BOTTLE (71335-1256-2)Feb 9, 2022
71335-1256-360 TABLET, FILM COATED in 1 BOTTLE (71335-1256-3)Feb 9, 2022
71335-1256-490 TABLET, FILM COATED in 1 BOTTLE (71335-1256-4)Feb 9, 2022
71335-1256-520 TABLET, FILM COATED in 1 BOTTLE (71335-1256-5)Feb 9, 2022
71335-1256-628 TABLET, FILM COATED in 1 BOTTLE (71335-1256-6)Feb 9, 2022
71335-1256-756 TABLET, FILM COATED in 1 BOTTLE (71335-1256-7)Feb 9, 2022
71335-1256-8180 TABLET, FILM COATED in 1 BOTTLE (71335-1256-8)Feb 9, 2022

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