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Methylphenidate Hydrochloride (LA)

NDC 0093-5347 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Generic nameMethylphenidate Hydrochloride
Labeler / ManufacturerTeva Pharmaceuticals USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA079031
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsMETHYLPHENIDATE HYDROCHLORIDE (30 mg/1)
Marketing started20120716
Package count1

External sources

Source: openFDA. Public-domain (CC0).