NDC 71335-9633 – Amitriptyline Hydrochloride

Amitriptyline Hydrochloride 25 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-9633

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
71335-9633-0120 TABLET, FILM COATED in 1 BOTTLE (71335-9633-0)Feb 6, 2023
71335-9633-120 TABLET, FILM COATED in 1 BOTTLE (71335-9633-1)Feb 6, 2023
71335-9633-230 TABLET, FILM COATED in 1 BOTTLE (71335-9633-2)Feb 6, 2023
71335-9633-3100 TABLET, FILM COATED in 1 BOTTLE (71335-9633-3)Feb 6, 2023
71335-9633-460 TABLET, FILM COATED in 1 BOTTLE (71335-9633-4)Feb 6, 2023
71335-9633-550 TABLET, FILM COATED in 1 BOTTLE (71335-9633-5)Feb 6, 2023
71335-9633-690 TABLET, FILM COATED in 1 BOTTLE (71335-9633-6)Feb 6, 2023
71335-9633-745 TABLET, FILM COATED in 1 BOTTLE (71335-9633-7)Feb 6, 2023
71335-9633-828 TABLET, FILM COATED in 1 BOTTLE (71335-9633-8)Feb 6, 2023
71335-9633-956 TABLET, FILM COATED in 1 BOTTLE (71335-9633-9)Feb 6, 2023

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