NDC 31722-173 – Methylphenidate Hydrochloride

Methylphenidate Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC31722-173

Product details

Brand name
Methylphenidate Hydrochloride
Generic name
Methylphenidate Hydrochloride
Labeler
Camber Pharmaceutical Inc
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA207416
Marketed since
October 1, 2015
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 (2)

Package NDCDescriptionSince
31722-173-01100 TABLET in 1 BOTTLE (31722-173-01)Oct 1, 2015
31722-173-05500 TABLET in 1 BOTTLE (31722-173-05)Oct 1, 2015

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