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METHYLPHENIDATE - 16590-837-60 - (METHYLPHENIDATE HYDROCHLORIDE)

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Drug Information of METHYLPHENIDATE

Product NDC: 16590-837
Proprietary Name: METHYLPHENIDATE
Non Proprietary Name: METHYLPHENIDATE HYDROCHLORIDE
Active Ingredient(s): 5    mg/1 & nbsp;   METHYLPHENIDATE HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of METHYLPHENIDATE

Product NDC: 16590-837
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040220
Marketing Category: ANDA
Start Marketing Date: 19970829

Package Information of METHYLPHENIDATE

Package NDC: 16590-837-60
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC (16590-837-60)

NDC Information of METHYLPHENIDATE

NDC Code 16590-837-60
Proprietary Name METHYLPHENIDATE
Package Description 60 TABLET in 1 BOTTLE, PLASTIC (16590-837-60)
Product NDC 16590-837
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name METHYLPHENIDATE HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19970829
Marketing Category Name ANDA
Labeler Name STAT RX USA LLC
Substance Name METHYLPHENIDATE HYDROCHLORIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE]

Complete Information of METHYLPHENIDATE


General Information