Ritalin - 0078-0370-05 - (methylphenidate hydrochloride)

Alphabetical Index


Drug Information of Ritalin

Product NDC: 0078-0370
Proprietary Name: Ritalin
Non Proprietary Name: methylphenidate hydrochloride
Active Ingredient(s): 20    mg/1 & nbsp;   methylphenidate hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Ritalin

Product NDC: 0078-0370
Labeler Name: Novartis Pharmaceuticals Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021284
Marketing Category: NDA
Start Marketing Date: 20020605

Package Information of Ritalin

Package NDC: 0078-0370-05
Package Description: 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0078-0370-05)

NDC Information of Ritalin

NDC Code 0078-0370-05
Proprietary Name Ritalin
Package Description 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0078-0370-05)
Product NDC 0078-0370
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name methylphenidate hydrochloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20020605
Marketing Category Name NDA
Labeler Name Novartis Pharmaceuticals Corporation
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 Ritalin


General Information