Home > National Drug Code (NDC) > Methylphenidate Hydrochloride

Methylphenidate Hydrochloride - 0093-5292-01 - (Methylphenidate Hydrochloride)

Alphabetical Index


Drug Information of Methylphenidate Hydrochloride

Product NDC: 0093-5292
Proprietary Name: Methylphenidate Hydrochloride
Non Proprietary Name: Methylphenidate Hydrochloride
Active Ingredient(s): 50    mg/1 & nbsp;   Methylphenidate Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Methylphenidate Hydrochloride

Product NDC: 0093-5292
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078873
Marketing Category: ANDA
Start Marketing Date: 20120927

Package Information of Methylphenidate Hydrochloride

Package NDC: 0093-5292-01
Package Description: 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-5292-01)

NDC Information of Methylphenidate Hydrochloride

NDC Code 0093-5292-01
Proprietary Name Methylphenidate Hydrochloride
Package Description 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-5292-01)
Product NDC 0093-5292
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Methylphenidate Hydrochloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20120927
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name METHYLPHENIDATE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE]

Complete Information of Methylphenidate Hydrochloride


General Information