NDC 68025-097 – Relexxii

Methylphenidate Hydrochloride 36 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug DEA schedule CII

Product NDC68025-097

Product details

Brand name
Relexxii
Generic name
methylphenidate hydrochloride
Labeler
Vertical Pharmaceuticals, LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
NDA · NDA216117
Marketed since
June 23, 2022
Listing expires
December 31, 2026
Pharmacologic class
Central Nervous System Stimulant

Active ingredients

Uses, dosage, side effects and warnings for Relexxii →

Package NDC codes (2)

Package NDCDescriptionSince
68025-097-10100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68025-097-10)Nov 1, 2023
68025-097-3030 TABLET, EXTENDED RELEASE in 1 BOTTLE (68025-097-30)Aug 12, 2024

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