Quillivant - 24478-205-25 - (METHYLPHENIDATE HYDROCHLORIDE)

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Drug Information of Quillivant

Product NDC: 24478-205
Proprietary Name: Quillivant
Non Proprietary Name: METHYLPHENIDATE HYDROCHLORIDE
Active Ingredient(s): 750    mg/150mL & nbsp;   METHYLPHENIDATE HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): POWDER, FOR SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Quillivant

Product NDC: 24478-205
Labeler Name: NextWave Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA202100
Marketing Category: NDA
Start Marketing Date: 20130104

Package Information of Quillivant

Package NDC: 24478-205-25
Package Description: 150 mL in 1 BOTTLE (24478-205-25)

NDC Information of Quillivant

NDC Code 24478-205-25
Proprietary Name Quillivant
Package Description 150 mL in 1 BOTTLE (24478-205-25)
Product NDC 24478-205
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name METHYLPHENIDATE HYDROCHLORIDE
Dosage Form Name POWDER, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 20130104
Marketing Category Name NDA
Labeler Name NextWave Pharmaceuticals, Inc.
Substance Name METHYLPHENIDATE HYDROCHLORIDE
Strength Number 750
Strength Unit mg/150mL
Pharmaceutical Classes Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE]

Complete Information of Quillivant


General Information