NDC 62037-725 – Methylphenidate Hydrochloride

Methylphenidate Hydrochloride 18 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug DEA schedule CII 2 recalls

Product NDC62037-725

Product details

Brand name
Methylphenidate Hydrochloride
Generic name
Methylphenidate Hydrochloride
Labeler
Actavis Pharma, Inc.
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA076772
Marketed since
March 4, 2019
Listing expires
December 31, 2027
Pharmacologic class
Central Nervous System Stimulant

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
62037-725-01100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62037-725-01)Mar 4, 2019

Recalls mentioning this NDC

Other Methylphenidate Hydrochloride products