NDC 43598-440 – Methylphenidate Hydrochloride

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

Human Prescription Drug DEA schedule CII

Product NDC43598-440

Product details

Brand name
Methylphenidate Hydrochloride
Generic name
Methylphenidate Hydrochloride
Labeler
Dr.Reddys Laboratories Inc
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA213473
Marketed since
August 20, 2020
Marketing end
September 30, 2026
Pharmacologic class
Central Nervous System Stimulant

Active ingredients

Uses, dosage, side effects and warnings for Methylphenidate Hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
43598-440-01100 TABLET, EXTENDED RELEASE in 1 BOTTLE (43598-440-01)Aug 20, 2020

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