NDC 71205-888 – Selegiline Hydrochloride

Selegiline Hydrochloride 5 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71205-888

Product details

Brand name
Selegiline Hydrochloride
Generic name
Selegiline Hydrochloride
Labeler
Proficient Rx LP
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 (6)

Package NDCDescriptionSince
71205-888-00100 CAPSULE in 1 BOTTLE (71205-888-00)Aug 3, 2021
71205-888-111000 CAPSULE in 1 BOTTLE (71205-888-11)Aug 3, 2021
71205-888-3030 CAPSULE in 1 BOTTLE (71205-888-30)Aug 3, 2021
71205-888-55500 CAPSULE in 1 BOTTLE (71205-888-55)Aug 3, 2021
71205-888-6060 CAPSULE in 1 BOTTLE (71205-888-60)Aug 3, 2021
71205-888-9090 CAPSULE in 1 BOTTLE (71205-888-90)Aug 3, 2021

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