Nucynta - 50458-817-02 - (tapentadol hydrochloride)

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Drug Information of Nucynta

Product NDC: 50458-817
Proprietary Name: Nucynta
Non Proprietary Name: tapentadol hydrochloride
Active Ingredient(s): 20    mg/mL & nbsp;   tapentadol hydrochloride
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Nucynta

Product NDC: 50458-817
Labeler Name: Janssen Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA203794
Marketing Category: NDA
Start Marketing Date: 20121015

Package Information of Nucynta

Package NDC: 50458-817-02
Package Description: 200 mL in 1 BOTTLE (50458-817-02)

NDC Information of Nucynta

NDC Code 50458-817-02
Proprietary Name Nucynta
Package Description 200 mL in 1 BOTTLE (50458-817-02)
Product NDC 50458-817
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name tapentadol hydrochloride
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20121015
Marketing Category Name NDA
Labeler Name Janssen Pharmaceuticals, Inc.
Substance Name TAPENTADOL HYDROCHLORIDE
Strength Number 20
Strength Unit mg/mL
Pharmaceutical Classes Opioid Agonist [EPC],Opioid Agonists [MoA]

Complete Information of Nucynta


General Information