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Dexmethylphenidate Hydrochloride - 0093-5275-01 - (Dexmethylphenidate Hydrochloride)

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Drug Information of Dexmethylphenidate Hydrochloride

Product NDC: 0093-5275
Proprietary Name: Dexmethylphenidate Hydrochloride
Non Proprietary Name: Dexmethylphenidate Hydrochloride
Active Ingredient(s): 2.5    mg/1 & nbsp;   Dexmethylphenidate Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Dexmethylphenidate Hydrochloride

Product NDC: 0093-5275
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077107
Marketing Category: ANDA
Start Marketing Date: 20070608

Package Information of Dexmethylphenidate Hydrochloride

Package NDC: 0093-5275-01
Package Description: 100 TABLET in 1 BOTTLE (0093-5275-01)

NDC Information of Dexmethylphenidate Hydrochloride

NDC Code 0093-5275-01
Proprietary Name Dexmethylphenidate Hydrochloride
Package Description 100 TABLET in 1 BOTTLE (0093-5275-01)
Product NDC 0093-5275
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dexmethylphenidate Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070608
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name DEXMETHYLPHENIDATE HYDROCHLORIDE
Strength Number 2.5
Strength Unit mg/1
Pharmaceutical Classes Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE]

Complete Information of Dexmethylphenidate Hydrochloride


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