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METHYLPHENIDATE HYDROCHLORIDE - 63629-3279-2 - (METHYLPHENIDATE HYDROCHLORIDE)

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Drug Information of METHYLPHENIDATE HYDROCHLORIDE

Product NDC: 63629-3279
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
Coding System: National Drug Codes(NDC)

Labeler Information of METHYLPHENIDATE HYDROCHLORIDE

Product NDC: 63629-3279
Labeler Name: bryant ranch prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040300
Marketing Category: ANDA
Start Marketing Date: 20100201

Package Information of METHYLPHENIDATE HYDROCHLORIDE

Package NDC: 63629-3279-2
Package Description: 90 TABLET in 1 BOTTLE (63629-3279-2)

NDC Information of METHYLPHENIDATE HYDROCHLORIDE

NDC Code 63629-3279-2
Proprietary Name METHYLPHENIDATE HYDROCHLORIDE
Package Description 90 TABLET in 1 BOTTLE (63629-3279-2)
Product NDC 63629-3279
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name METHYLPHENIDATE HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100201
Marketing Category Name ANDA
Labeler Name bryant ranch prepack
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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