NDC 57664-687 – Amitriptyline Hydrochloride

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

Human Prescription Drug

Product NDC57664-687

Product details

Brand name
Amitriptyline Hydrochloride
Generic name
Amitriptyline Hydrochloride
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA089399
Marketed since
July 14, 1987
Listing expires
December 31, 2027
Pharmacologic class
Tricyclic Antidepressant

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
57664-687-181000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (57664-687-18)Jul 14, 1987
57664-687-88100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (57664-687-88)Jul 14, 1987

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