NDC 13107-380 – Methylphenidate Hydrochloride

Methylphenidate Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC13107-380

Product details

Brand name
Methylphenidate Hydrochloride
Generic name
Methylphenidate Hydrochloride
Labeler
Aurolife Pharma, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA209276
Marketed since
April 11, 2017
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
13107-380-01100 TABLET in 1 BOTTLE (13107-380-01)Apr 11, 2017

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