NDC 71335-2673 – Selegiline Hydrochloride

Selegiline Hydrochloride 5 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-2673

Product details

Brand name
Selegiline Hydrochloride
Generic name
Selegiline Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA206803
Marketed since
April 2, 2019
Listing expires
December 31, 2026
Pharmacologic class
Monoamine Oxidase Inhibitor; Monoamine Oxidase Type B Inhibitor

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
71335-2673-130 CAPSULE in 1 BOTTLE (71335-2673-1)Jul 15, 2025

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