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Methylphenidate Hydrochloride - 60429-579-01 - (Methylphenidate Hydrochloride)

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Drug Information of Methylphenidate Hydrochloride

Product NDC: 60429-579
Proprietary Name: Methylphenidate Hydrochloride
Non Proprietary Name: Methylphenidate Hydrochloride
Active Ingredient(s): 10    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: 60429-579
Labeler Name: Golden State Medical Supply, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075629
Marketing Category: ANDA
Start Marketing Date: 20100520

Package Information of Methylphenidate Hydrochloride

Package NDC: 60429-579-01
Package Description: 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (60429-579-01)

NDC Information of Methylphenidate Hydrochloride

NDC Code 60429-579-01
Proprietary Name Methylphenidate Hydrochloride
Package Description 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (60429-579-01)
Product NDC 60429-579
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Methylphenidate Hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20100520
Marketing Category Name ANDA
Labeler Name Golden State Medical Supply, Inc.
Substance Name METHYLPHENIDATE HYDROCHLORIDE
Strength Number 10
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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