NDC 72319-006 – Selegiline Hydrochloride

Selegiline Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72319-006

Product details

Brand name
Selegiline Hydrochloride
Generic name
Selegiline Hydrochloride
Labeler
i3 Pharmaceuticals, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA074672
Marketed since
December 15, 2021
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
72319-006-0260 TABLET in 1 BOTTLE (72319-006-02)Dec 15, 2021

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