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Methylphenidate Hydrochloride - 0781-5748-01 - (methylphenidate hydrochloride)

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Drug Information of Methylphenidate Hydrochloride

Product NDC: 0781-5748
Proprietary Name: Methylphenidate Hydrochloride
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 Hydrochloride

Product NDC: 0781-5748
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA010187
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 19551231

Package Information of Methylphenidate Hydrochloride

Package NDC: 0781-5748-01
Package Description: 100 TABLET in 1 BOTTLE (0781-5748-01)

NDC Information of Methylphenidate Hydrochloride

NDC Code 0781-5748-01
Proprietary Name Methylphenidate Hydrochloride
Package Description 100 TABLET in 1 BOTTLE (0781-5748-01)
Product NDC 0781-5748
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name methylphenidate hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19551231
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Sandoz Inc
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 Hydrochloride


General Information