NDC 31722-954 – Methylphenidate Hydrochloride

Methylphenidate Hydrochloride 36 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug DEA schedule CII

Product NDC31722-954

Product details

Brand name
Methylphenidate Hydrochloride
Generic name
Methylphenidate Hydrochloride
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA211009
Marketed since
September 3, 2019
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
31722-954-01100 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-954-01)Sep 3, 2019

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