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Metadate ER - 53014-594-07 - (methylphenidate hydrochloride)

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Drug Information of Metadate ER

Product NDC: 53014-594
Proprietary Name: Metadate ER
Non Proprietary Name: methylphenidate hydrochloride
Active Ingredient(s): 20    mg/1 & nbsp;   methylphenidate hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Metadate ER

Product NDC: 53014-594
Labeler Name: UCB Manufacturing, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089601
Marketing Category: ANDA
Start Marketing Date: 19880601

Package Information of Metadate ER

Package NDC: 53014-594-07
Package Description: 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (53014-594-07)

NDC Information of Metadate ER

NDC Code 53014-594-07
Proprietary Name Metadate ER
Package Description 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (53014-594-07)
Product NDC 53014-594
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name methylphenidate hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19880601
Marketing Category Name ANDA
Labeler Name UCB Manufacturing, 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 Metadate ER


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