NDC 75834-324 – Methylphenidate Hydrochloride

Methylphenidate Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC75834-324

Product details

Brand name
Methylphenidate Hydrochloride
Generic name
Methylphenidate Hydrochloride
Labeler
Nivagen Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA208737
Marketed since
April 16, 2024
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
75834-324-01100 TABLET in 1 BOTTLE (75834-324-01)Apr 16, 2024

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