NDC 71335-0395 – Amitriptyline Hydrochloride

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

Human Prescription Drug

Product NDC71335-0395

Product details

Brand name
Amitriptyline Hydrochloride
Generic name
Amitriptyline Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202446
Marketed since
December 5, 2014
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
71335-0395-0100 TABLET, FILM COATED in 1 BOTTLE (71335-0395-0)Dec 5, 2014
71335-0395-130 TABLET, FILM COATED in 1 BOTTLE (71335-0395-1)Dec 5, 2014
71335-0395-215 TABLET, FILM COATED in 1 BOTTLE (71335-0395-2)Dec 5, 2014
71335-0395-360 TABLET, FILM COATED in 1 BOTTLE (71335-0395-3)Dec 5, 2014
71335-0395-490 TABLET, FILM COATED in 1 BOTTLE (71335-0395-4)Dec 5, 2014
71335-0395-528 TABLET, FILM COATED in 1 BOTTLE (71335-0395-5)Dec 5, 2014
71335-0395-6120 TABLET, FILM COATED in 1 BOTTLE (71335-0395-6)Dec 5, 2014
71335-0395-750 TABLET, FILM COATED in 1 BOTTLE (71335-0395-7)Dec 5, 2014
71335-0395-8180 TABLET, FILM COATED in 1 BOTTLE (71335-0395-8)Dec 5, 2014
71335-0395-96 TABLET, FILM COATED in 1 BOTTLE (71335-0395-9)Dec 5, 2014

Other Amitriptyline Hydrochloride products