NDC 75834-327 – Dexmethylphenidate hydrochloride

Dexmethylphenidate Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC75834-327

Product details

Brand name
Dexmethylphenidate hydrochloride
Generic name
Dexmethylphenidate hydrochloride
Labeler
Nivagen Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA209211
Marketed since
May 3, 2024
Listing expires
December 31, 2027
Pharmacologic class
Central Nervous System Stimulant

Active ingredients

Uses, dosage, side effects and warnings for Dexmethylphenidate Hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
75834-327-01100 TABLET in 1 BOTTLE (75834-327-01)May 3, 2024

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