NDC 71335-2350 – Nortriptyline Hydrochloride

Nortriptyline Hydrochloride 25 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-2350

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 (7)

Package NDCDescriptionSince
71335-2350-260 CAPSULE in 1 BOTTLE, PLASTIC (71335-2350-2)Feb 21, 2024
71335-2350-430 CAPSULE in 1 BOTTLE, PLASTIC (71335-2350-4)Feb 21, 2024
71335-2350-590 CAPSULE in 1 BOTTLE, PLASTIC (71335-2350-5)Feb 21, 2024
71335-2350-650 CAPSULE in 1 BOTTLE, PLASTIC (71335-2350-6)Feb 21, 2024
71335-2350-7100 CAPSULE in 1 BOTTLE, PLASTIC (71335-2350-7)Feb 21, 2024
71335-2350-8120 CAPSULE in 1 BOTTLE, PLASTIC (71335-2350-8)Feb 21, 2024
71335-2350-928 CAPSULE in 1 BOTTLE, PLASTIC (71335-2350-9)Feb 21, 2024

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