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Methylphenidate Hydrochloride - 0781-5754-01 - (methylphenidate hydrochloride)

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Drug Information of Methylphenidate Hydrochloride

Product NDC: 0781-5754
Proprietary Name: Methylphenidate Hydrochloride
Non Proprietary Name: methylphenidate hydrochloride
Active Ingredient(s): 20    mg/1 & nbsp;   methylphenidate hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Methylphenidate Hydrochloride

Product NDC: 0781-5754
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018029
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 19820331

Package Information of Methylphenidate Hydrochloride

Package NDC: 0781-5754-01
Package Description: 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0781-5754-01)

NDC Information of Methylphenidate Hydrochloride

NDC Code 0781-5754-01
Proprietary Name Methylphenidate Hydrochloride
Package Description 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0781-5754-01)
Product NDC 0781-5754
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name methylphenidate hydrochloride
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19820331
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Sandoz 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 Methylphenidate Hydrochloride


General Information