NDC 71335-2351 – Nortriptyline Hydrochloride

Nortriptyline Hydrochloride 50 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-2351

Product details

Brand name
Nortriptyline Hydrochloride
Generic name
Nortriptyline Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA073556
Marketed since
November 17, 2023
Listing expires
December 31, 2026
Pharmacologic class
Tricyclic Antidepressant

Active ingredients

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

Package NDC codes (5)

Package NDCDescriptionSince
71335-2351-130 CAPSULE in 1 BOTTLE, PLASTIC (71335-2351-1)Feb 21, 2024
71335-2351-260 CAPSULE in 1 BOTTLE, PLASTIC (71335-2351-2)Feb 21, 2024
71335-2351-390 CAPSULE in 1 BOTTLE, PLASTIC (71335-2351-3)Feb 21, 2024
71335-2351-428 CAPSULE in 1 BOTTLE, PLASTIC (71335-2351-4)Feb 21, 2024
71335-2351-5120 CAPSULE in 1 BOTTLE, PLASTIC (71335-2351-5)Feb 21, 2024

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