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Methylphenidate Hydrochloride - 54868-3454-4 - (methylphenidate hydrochloride)

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Drug Information of Methylphenidate Hydrochloride

Product NDC: 54868-3454
Proprietary Name: Methylphenidate Hydrochloride
Non Proprietary Name: methylphenidate hydrochloride
Active Ingredient(s): 20    mg/1 & nbsp;   methylphenidate hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Methylphenidate Hydrochloride

Product NDC: 54868-3454
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA086428
Marketing Category: ANDA
Start Marketing Date: 19941216

Package Information of Methylphenidate Hydrochloride

Package NDC: 54868-3454-4
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-3454-4)

NDC Information of Methylphenidate Hydrochloride

NDC Code 54868-3454-4
Proprietary Name Methylphenidate Hydrochloride
Package Description 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-3454-4)
Product NDC 54868-3454
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name methylphenidate hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19941216
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 Hydrochloride


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