Ritalin - 54868-2762-0 - (methylphenidate hydrochloride)

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Drug Information of Ritalin

Product NDC: 54868-2762
Proprietary Name: Ritalin
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 Ritalin

Product NDC: 54868-2762
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA010187
Marketing Category: NDA
Start Marketing Date: 20000310

Package Information of Ritalin

Package NDC: 54868-2762-0
Package Description: 60 TABLET in 1 BOTTLE (54868-2762-0)

NDC Information of Ritalin

NDC Code 54868-2762-0
Proprietary Name Ritalin
Package Description 60 TABLET in 1 BOTTLE (54868-2762-0)
Product NDC 54868-2762
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name methylphenidate hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20000310
Marketing Category Name NDA
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 Ritalin


General Information