NDC 0078-0371 – Ritalin LA

Methylphenidate Hydrochloride 30 mg/1 · Capsule, Extended Release · Oral

Human Prescription Drug DEA schedule CII

Product NDC0078-0371

Product details

Brand name
Ritalin LA
Generic name
Methylphenidate hydrochloride
Labeler
Novartis Pharmaceuticals Corporation
Dosage form
Capsule, Extended Release
Route
Oral
Marketing category
NDA · NDA021284
Marketed since
June 5, 2002
Marketing end
October 31, 2026
Pharmacologic class
Central Nervous System Stimulant

Active ingredients

Uses, dosage, side effects and warnings for Ritalin →

Package NDC codes (1)

Package NDCDescriptionSince
0078-0371-05100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0078-0371-05)Jun 5, 2002

Other Ritalin products