NDC 42806-097 – Protriptyline Hydrochloride

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

Human Prescription Drug

Product NDC42806-097

Product details

Brand name
Protriptyline Hydrochloride
Generic name
Protriptyline Hydrochloride
Labeler
Epic Pharma, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202220
Marketed since
January 9, 2013
Listing expires
December 31, 2026
Pharmacologic class
Tricyclic Antidepressant

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
42806-097-01100 TABLET, FILM COATED in 1 BOTTLE (42806-097-01)Jan 9, 2013
42806-097-101000 TABLET, FILM COATED in 1 BOTTLE (42806-097-10)Jan 9, 2013
42806-097-3030 TABLET, FILM COATED in 1 BOTTLE (42806-097-30)Jul 10, 2020

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