NDC 16729-480 – Methylphenidate Hydrochloride

Methylphenidate Hydrochloride 20 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC16729-480

Product details

Brand name
Methylphenidate Hydrochloride
Generic name
Methylphenidate Hydrochloride
Labeler
Accord Healthcare, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA213936
Marketed since
December 17, 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
16729-480-01100 TABLET in 1 BOTTLE (16729-480-01)Dec 17, 2020

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