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Metadate CD - 53014-579-07 - (methylphenidate hydrochloride)

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Drug Information of Metadate CD

Product NDC: 53014-579
Proprietary Name: Metadate CD
Non Proprietary Name: methylphenidate hydrochloride
Active Ingredient(s): 10    mg/1 & nbsp;   methylphenidate hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Metadate CD

Product NDC: 53014-579
Labeler Name: UCB Manufacturing, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021259
Marketing Category: NDA
Start Marketing Date: 20030812

Package Information of Metadate CD

Package NDC: 53014-579-07
Package Description: 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (53014-579-07)

NDC Information of Metadate CD

NDC Code 53014-579-07
Proprietary Name Metadate CD
Package Description 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (53014-579-07)
Product NDC 53014-579
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name methylphenidate hydrochloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20030812
Marketing Category Name NDA
Labeler Name UCB Manufacturing, Inc.
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 Metadate CD


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