NDC 0406-1144 – Methylphenidate Hydrochloride

Methylphenidate Hydrochloride 10 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC0406-1144

Product details

Brand name
Methylphenidate Hydrochloride
Generic name
Methylphenidate Hydrochloride
Labeler
SpecGx LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040300
Marketed since
November 27, 1998
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
0406-1144-01100 TABLET in 1 BOTTLE (0406-1144-01)Nov 27, 1998
0406-1144-101000 TABLET in 1 BOTTLE (0406-1144-10)Nov 27, 1998

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