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Methylphenidate Hydrochloride - 54868-6261-1 - (Methylphenidate Hydrochloride)

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Drug Information of Methylphenidate Hydrochloride

Product NDC: 54868-6261
Proprietary Name: Methylphenidate Hydrochloride
Non Proprietary Name: Methylphenidate Hydrochloride
Active Ingredient(s): 18    mg/1 & nbsp;   Methylphenidate Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Methylphenidate Hydrochloride

Product NDC: 54868-6261
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021121
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20110601

Package Information of Methylphenidate Hydrochloride

Package NDC: 54868-6261-1
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (54868-6261-1)

NDC Information of Methylphenidate Hydrochloride

NDC Code 54868-6261-1
Proprietary Name Methylphenidate Hydrochloride
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (54868-6261-1)
Product NDC 54868-6261
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Methylphenidate Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110601
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Physicians Total Care, Inc.
Substance Name METHYLPHENIDATE HYDROCHLORIDE
Strength Number 18
Strength Unit mg/1
Pharmaceutical Classes Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE]

Complete Information of Methylphenidate Hydrochloride


General Information