NDC 57664-228 – Methylphenidate Hydrochloride

Methylphenidate Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII 1 recall

Product NDC57664-228

Product details

Brand name
Methylphenidate Hydrochloride
Generic name
Methylphenidate Hydrochloride
Labeler
Sun Pharmaceutical Industries, Inc.
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 (5)

Package NDCDescriptionSince
57664-228-08100 TABLET in 1 BOTTLE (57664-228-08)Aug 16, 2013
57664-228-13500 TABLET in 1 BOTTLE (57664-228-13)Aug 16, 2013
57664-228-181000 TABLET in 1 BOTTLE (57664-228-18)Aug 16, 2013
57664-228-8330 TABLET in 1 BOTTLE (57664-228-83)Aug 16, 2013
57664-228-88100 TABLET in 1 BOTTLE (57664-228-88)Aug 16, 2013

Recalls mentioning this NDC

Other Methylphenidate Hydrochloride products