NDC 71610-752 – Amitriptyline Hydrochloride

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

Human Prescription Drug

Product NDC71610-752

Product details

Brand name
Amitriptyline Hydrochloride
Generic name
Amitriptyline Hydrochloride
Labeler
Aphena Pharma Solutions - Tennessee, LLC
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 (4)

Package NDCDescriptionSince
71610-752-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-752-30)Nov 13, 2023
71610-752-5360 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-752-53)Nov 13, 2023
71610-752-6090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-752-60)Nov 13, 2023
71610-752-80180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-752-80)Nov 13, 2023

Other Amitriptyline Hydrochloride products