NDC 51672-4001 – Nortriptyline Hydrochloride

Nortriptyline Hydrochloride 10 mg/1 · Capsule · Oral

Human Prescription Drug 1 recall

Product NDC51672-4001

Product details

Brand name
Nortriptyline Hydrochloride
Generic name
Nortriptyline Hydrochloride
Labeler
Sun Pharmaceutical Industries, Inc.
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 (4)

Package NDCDescriptionSince
51672-4001-1100 CAPSULE in 1 BOTTLE (51672-4001-1)May 8, 2000
51672-4001-2500 CAPSULE in 1 BOTTLE (51672-4001-2)May 8, 2000
51672-4001-590 CAPSULE in 1 BOTTLE (51672-4001-5)May 8, 2000
51672-4001-630 CAPSULE in 1 BOTTLE (51672-4001-6)May 8, 2000

Recalls mentioning this NDC

Other Nortriptyline Hydrochloride products