Methylin - 60429-538-01 - (Methylphenidate Hydrochloride)

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Drug Information of Methylin

Product NDC: 60429-538
Proprietary Name: Methylin
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 Methylin

Product NDC: 60429-538
Labeler Name: Golden State Medical Supply, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040300
Marketing Category: ANDA
Start Marketing Date: 20100520

Package Information of Methylin

Package NDC: 60429-538-01
Package Description: 100 TABLET in 1 BOTTLE (60429-538-01)

NDC Information of Methylin

NDC Code 60429-538-01
Proprietary Name Methylin
Package Description 100 TABLET in 1 BOTTLE (60429-538-01)
Product NDC 60429-538
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Methylphenidate Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100520
Marketing Category Name ANDA
Labeler Name Golden State Medical Supply, 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 Methylin


General Information