NDC 57664-710 – Methylphenidate Hydrochloride

Methylphenidate Hydrochloride 72 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug DEA schedule CII

Product NDC57664-710

Product details

Brand name
Methylphenidate Hydrochloride
Generic name
Methylphenidate Hydrochloride
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA217229
Marketed since
December 20, 2024
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 (2)

Package NDCDescriptionSince
57664-710-8330 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (57664-710-83)Dec 20, 2024
57664-710-88100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (57664-710-88)Dec 20, 2024

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