Home > National Drug Code (NDC) > methylphenidate hydrochloride CD

methylphenidate hydrochloride CD - 62175-154-37 - (methylphenidate hydrochloride)

Alphabetical Index


Drug Information of methylphenidate hydrochloride CD

Product NDC: 62175-154
Proprietary Name: methylphenidate hydrochloride CD
Non Proprietary Name: methylphenidate hydrochloride
Active Ingredient(s): 40    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 CD

Product NDC: 62175-154
Labeler Name: Kremers Urban Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021259
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20060321

Package Information of methylphenidate hydrochloride CD

Package NDC: 62175-154-37
Package Description: 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62175-154-37)

NDC Information of methylphenidate hydrochloride CD

NDC Code 62175-154-37
Proprietary Name methylphenidate hydrochloride CD
Package Description 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62175-154-37)
Product NDC 62175-154
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name methylphenidate hydrochloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20060321
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Kremers Urban Pharmaceuticals Inc.
Substance Name METHYLPHENIDATE HYDROCHLORIDE
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE]

Complete Information of methylphenidate hydrochloride CD


General Information