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NDC 00527-1899-01 Dexmethylphenidate Hydrochloride 2.5 mg/1 Details

Dexmethylphenidate Hydrochloride 2.5 mg/1

Dexmethylphenidate Hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Lannett Company, Inc.. The primary component is DEXMETHYLPHENIDATE HYDROCHLORIDE.

MedlinePlus Drug Summary

Dexmethylphenidate is used as part of a treatment program to control symptoms of attention deficit hyperactivity disorder (ADHD; more difficulty focusing, controlling actions, and remaining still or quiet than other people who are the same age) in adults and children. Dexmethylphenidate is in a class of medications called central nervous system (CNS) stimulants. It works by increasing the amounts of certain natural substances in the brain.

Related Packages: 00527-1899-01
Last Updated: 03/24/2024
MedLinePlus Full Drug Details: Dexmethylphenidate

Product Information

NDC	00527-1899
Product ID	0527-1899_4edb2085-e7e1-4f52-a8fe-dd3bc175c052
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Dexmethylphenidate Hydrochloride
Proprietary Name Suffix	n/a
Non-Proprietary Name	Dexmethylphenidate Hydrochloride
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET
Route	ORAL
Active Ingredient Strength	2.5
Active Ingredient Units	mg/1
Substance Name	DEXMETHYLPHENIDATE HYDROCHLORIDE
Labeler Name	Lannett Company, Inc.
Pharmaceutical Class	Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE]
DEA Schedule	CII
Marketing Category	ANDA
Application Number	ANDA209468
Listing Certified Through	2024-12-31

Package

NDC 00527-1899-01 (00527189901)

Pricing Information	N/A
NDC Package Code	0527-1899-01
Billing NDC	00527189901
Package	100 TABLET in 1 BOTTLE (0527-1899-01)
Marketing Start Date	2017-09-25
NDC Exclude Flag	N