Concerta - 54868-4759-2 - (Methylphenidate hydrochloride)

Alphabetical Index


Drug Information of Concerta

Product NDC: 54868-4759
Proprietary Name: Concerta
Non Proprietary Name: Methylphenidate hydrochloride
Active Ingredient(s): 36    mg/1 & nbsp;   Methylphenidate hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Concerta

Product NDC: 54868-4759
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021121
Marketing Category: NDA
Start Marketing Date: 20030320

Package Information of Concerta

Package NDC: 54868-4759-2
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-4759-2)

NDC Information of Concerta

NDC Code 54868-4759-2
Proprietary Name Concerta
Package Description 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-4759-2)
Product NDC 54868-4759
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Methylphenidate hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20030320
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name METHYLPHENIDATE HYDROCHLORIDE
Strength Number 36
Strength Unit mg/1
Pharmaceutical Classes Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE]

Complete Information of Concerta


General Information