Concerta - 54868-4957-0 - (Methylphenidate hydrochloride)

Alphabetical Index


Drug Information of Concerta

Product NDC: 54868-4957
Proprietary Name: Concerta
Non Proprietary Name: Methylphenidate hydrochloride
Active Ingredient(s): 27    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: 54868-4957
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021121
Marketing Category: NDA
Start Marketing Date: 20031113

Package Information of Concerta

Package NDC: 54868-4957-0
Package Description: 10 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-4957-0)

NDC Information of Concerta

NDC Code 54868-4957-0
Proprietary Name Concerta
Package Description 10 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-4957-0)
Product NDC 54868-4957
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Methylphenidate hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20031113
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name METHYLPHENIDATE HYDROCHLORIDE
Strength Number 27
Strength Unit mg/1
Pharmaceutical Classes Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE]

Complete Information of Concerta


General Information