NDC 0093-0812 – Nortriptyline Hydrochloride

Nortriptyline Hydrochloride 50 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC0093-0812

Product details

Brand name
Nortriptyline Hydrochloride
Generic name
Nortriptyline Hydrochloride
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA074132
Marketed since
April 5, 1995
Listing expires
December 31, 2026
Pharmacologic class
Tricyclic Antidepressant

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
0093-0812-01100 CAPSULE in 1 BOTTLE (0093-0812-01)Apr 5, 1995
0093-0812-05500 CAPSULE in 1 BOTTLE (0093-0812-05)Apr 6, 1995

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