NDC 72865-122 – Methylphenidate Hydrochloride

Methylphenidate Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC72865-122

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
72865-122-01100 TABLET in 1 BOTTLE (72865-122-01)Feb 26, 2020
72865-122-05500 TABLET in 1 BOTTLE (72865-122-05)Feb 26, 2020

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