NDC 72865-123 – Methylphenidate Hydrochloride

Methylphenidate Hydrochloride 10 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC72865-123

Product details

Brand name
Methylphenidate Hydrochloride
Generic name
Methylphenidate Hydrochloride
Labeler
XLCare Pharmaceuticals Inc
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA207416
Marketed since
February 26, 2020
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 (2)

Package NDCDescriptionSince
72865-123-01100 TABLET in 1 BOTTLE (72865-123-01)Feb 26, 2020
72865-123-05500 TABLET in 1 BOTTLE (72865-123-05)Feb 26, 2020

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