NDC 72162-1636 – Methylphenidate Hydrochloride

Methylphenidate Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC72162-1636

Product details

Brand name
Methylphenidate Hydrochloride
Generic name
Methylphenidate Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA090710
Marketed since
August 16, 2013
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 (1)

Package NDCDescriptionSince
72162-1636-1100 TABLET in 1 BOTTLE (72162-1636-1)Aug 16, 2013

Other Methylphenidate Hydrochloride products