NDC 16571-659 – Selegiline Hydrochloride

Selegiline Hydrochloride 5 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC16571-659

Product details

Brand name
Selegiline Hydrochloride
Generic name
Selegiline Hydrochloride
Labeler
Rising Pharma Holdings, Inc.
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 (2)

Package NDCDescriptionSince
16571-659-0660 CAPSULE in 1 BOTTLE (16571-659-06)Apr 2, 2019
16571-659-50500 CAPSULE in 1 BOTTLE (16571-659-50)Apr 2, 2019

Other Selegiline Hydrochloride products