NDC 71335-9637 – Amitriptyline Hydrochloride

Amitriptyline Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-9637

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 (10)

Package NDCDescriptionSince
71335-9637-0100 TABLET, FILM COATED in 1 BOTTLE (71335-9637-0)Feb 6, 2023
71335-9637-130 TABLET, FILM COATED in 1 BOTTLE (71335-9637-1)Feb 6, 2023
71335-9637-215 TABLET, FILM COATED in 1 BOTTLE (71335-9637-2)Feb 6, 2023
71335-9637-360 TABLET, FILM COATED in 1 BOTTLE (71335-9637-3)Feb 6, 2023
71335-9637-490 TABLET, FILM COATED in 1 BOTTLE (71335-9637-4)Feb 6, 2023
71335-9637-528 TABLET, FILM COATED in 1 BOTTLE (71335-9637-5)Feb 6, 2023
71335-9637-6120 TABLET, FILM COATED in 1 BOTTLE (71335-9637-6)Feb 6, 2023
71335-9637-750 TABLET, FILM COATED in 1 BOTTLE (71335-9637-7)Feb 6, 2023
71335-9637-8180 TABLET, FILM COATED in 1 BOTTLE (71335-9637-8)Feb 6, 2023
71335-9637-96 TABLET, FILM COATED in 1 BOTTLE (71335-9637-9)Feb 6, 2023

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