NDC 71335-0426 – Nortriptyline Hydrochloride

Nortriptyline Hydrochloride 10 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-0426

Product details

Brand name
Nortriptyline Hydrochloride
Generic name
Nortriptyline Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA075520
Marketed since
May 8, 2000
Listing expires
December 31, 2027
Pharmacologic class
Tricyclic Antidepressant

Active ingredients

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

Package NDC codes (6)

Package NDCDescriptionSince
71335-0426-130 CAPSULE in 1 BOTTLE (71335-0426-1)Apr 29, 2015
71335-0426-260 CAPSULE in 1 BOTTLE (71335-0426-2)Apr 29, 2015
71335-0426-390 CAPSULE in 1 BOTTLE (71335-0426-3)Apr 29, 2015
71335-0426-4100 CAPSULE in 1 BOTTLE (71335-0426-4)Apr 29, 2015
71335-0426-5120 CAPSULE in 1 BOTTLE (71335-0426-5)Apr 29, 2015
71335-0426-615 CAPSULE in 1 BOTTLE (71335-0426-6)Apr 29, 2015

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