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Methylphenidate - 54868-2974-1 - (methylphenidate hydrochloride)

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Drug Information of Methylphenidate

Product NDC: 54868-2974
Proprietary Name: Methylphenidate
Non Proprietary Name: methylphenidate hydrochloride
Active Ingredient(s): 20    mg/1 & nbsp;   methylphenidate hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Methylphenidate

Product NDC: 54868-2974
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040220
Marketing Category: ANDA
Start Marketing Date: 20071016

Package Information of Methylphenidate

Package NDC: 54868-2974-1
Package Description: 20 TABLET in 1 BOTTLE (54868-2974-1)

NDC Information of Methylphenidate

NDC Code 54868-2974-1
Proprietary Name Methylphenidate
Package Description 20 TABLET in 1 BOTTLE (54868-2974-1)
Product NDC 54868-2974
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name methylphenidate hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20071016
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name METHYLPHENIDATE HYDROCHLORIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE]

Complete Information of Methylphenidate


General Information