NDC 51407-528 – Methylphenidate Hydrochloride

Methylphenidate Hydrochloride 20 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug DEA schedule CII

Product NDC51407-528

Product details

Brand name
Methylphenidate Hydrochloride
Generic name
Methylphenidate Hydrochloride
Labeler
Golden State Medical Supply, Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA210992
Marketed since
November 21, 2018
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
51407-528-01100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51407-528-01)Nov 14, 2019

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