NDC 0121-0678 – Nortriptyline Hydrochloride

Nortriptyline Hydrochloride 10 mg/5mL · Solution · Oral

Human Prescription Drug

Product NDC0121-0678

Product details

Brand name
Nortriptyline Hydrochloride
Generic name
Nortriptyline Hydrochloride
Labeler
PAI Holdings, LLC dba PAI Pharma
Dosage form
Solution
Route
Oral
Marketing category
ANDA · ANDA075606
Marketed since
August 23, 2000
Listing expires
December 31, 2027
Pharmacologic class
Tricyclic Antidepressant

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
0121-0678-16473 mL in 1 BOTTLE (0121-0678-16)Aug 23, 2000

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