Methylin - 59630-755-50 - (Methylphenidate Hydrochloride)

Alphabetical Index


Drug Information of Methylin

Product NDC: 59630-755
Proprietary Name: Methylin
Non Proprietary Name: Methylphenidate Hydrochloride
Active Ingredient(s): 10    mg/5mL & nbsp;   Methylphenidate Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Methylin

Product NDC: 59630-755
Labeler Name: SHIONOGI INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021419
Marketing Category: NDA
Start Marketing Date: 20101101

Package Information of Methylin

Package NDC: 59630-755-50
Package Description: 500 mL in 1 BOTTLE (59630-755-50)

NDC Information of Methylin

NDC Code 59630-755-50
Proprietary Name Methylin
Package Description 500 mL in 1 BOTTLE (59630-755-50)
Product NDC 59630-755
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Methylphenidate Hydrochloride
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20101101
Marketing Category Name NDA
Labeler Name SHIONOGI INC.
Substance Name METHYLPHENIDATE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/5mL
Pharmaceutical Classes Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE]

Complete Information of Methylin


General Information