NDC 0781-1488 – Amitriptyline Hydrochloride

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

Human Prescription Drug 1 recall

Product NDC0781-1488

Product details

Brand name
Amitriptyline Hydrochloride
Generic name
Amitriptyline Hydrochloride
Labeler
Sandoz Inc
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA085968
Marketed since
November 29, 1977
Listing expires
December 31, 2026
Pharmacologic class
Tricyclic Antidepressant

Active ingredients

Uses, dosage, side effects and warnings for Amitriptyline Hydrochloride →

Package NDC codes (2)

Package NDCDescriptionSince
0781-1488-01100 TABLET, FILM COATED in 1 BOTTLE (0781-1488-01)Nov 29, 1977
0781-1488-101000 TABLET, FILM COATED in 1 BOTTLE (0781-1488-10)Nov 29, 1977

Recalls mentioning this NDC

Other Amitriptyline Hydrochloride products