NDC 0406-1820 – Methylphenidate Hydrochloride Extended-Release

Methylphenidate Hydrochloride 20 mg/1 · Capsule, Extended Release · Oral

Human Prescription Drug DEA schedule CII

Product NDC0406-1820

Product details

Brand name
Methylphenidate Hydrochloride Extended-Release
Generic name
Methylphenidate hydrochloride
Labeler
SpecGx LLC
Dosage form
Capsule, Extended Release
Route
Oral
Marketing category
ANDA · ANDA203583
Marketed since
September 29, 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 (1)

Package NDCDescriptionSince
0406-1820-01100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0406-1820-01)Sep 29, 2015

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