NDC 71335-1219 – Methylphenidate Hydrochloride

Methylphenidate Hydrochloride 20 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC71335-1219

Product details

Brand name
Methylphenidate Hydrochloride
Generic name
Methylphenidate Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA207416
Marketed since
October 1, 2015
Listing expires
December 31, 2026
Pharmacologic class
Central Nervous System Stimulant

Active ingredients

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

Package NDC codes (5)

Package NDCDescriptionSince
71335-1219-130 TABLET in 1 BOTTLE (71335-1219-1)Oct 31, 2024
71335-1219-2100 TABLET in 1 BOTTLE (71335-1219-2)Oct 31, 2024
71335-1219-390 TABLET in 1 BOTTLE (71335-1219-3)Apr 24, 2019
71335-1219-460 TABLET in 1 BOTTLE (71335-1219-4)Apr 24, 2019
71335-1219-5120 TABLET in 1 BOTTLE (71335-1219-5)Oct 31, 2024

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