NDC 10135-737 – Selegiline Hydrochloride

Selegiline Hydrochloride 5 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC10135-737

Product details

Brand name
Selegiline Hydrochloride
Generic name
Selegiline Hydrochloride
Labeler
Marlex Pharmaceuticals, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA075352
Marketed since
May 1, 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
10135-737-6060 CAPSULE in 1 BOTTLE (10135-737-60)May 1, 2021

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