NDC 60687-543 – Methylphenidate Hydrochloride

Methylphenidate Hydrochloride 27 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug DEA schedule CII

Product NDC60687-543

Product details

Brand name
Methylphenidate Hydrochloride
Generic name
Methylphenidate Hydrochloride
Labeler
American Health Packaging
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA211009
Marketed since
June 25, 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 (1)

Package NDCDescriptionSince
60687-543-2130 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-543-21) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-543-11)Jun 25, 2020

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