Nucynta - 54868-5979-0 - (tapentadol hydrochloride)

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Drug Information of Nucynta

Product NDC: 54868-5979
Proprietary Name: Nucynta
Non Proprietary Name: tapentadol hydrochloride
Active Ingredient(s): 50    mg/1 & nbsp;   tapentadol hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Nucynta

Product NDC: 54868-5979
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022304
Marketing Category: NDA
Start Marketing Date: 20100319

Package Information of Nucynta

Package NDC: 54868-5979-0
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (54868-5979-0)

NDC Information of Nucynta

NDC Code 54868-5979-0
Proprietary Name Nucynta
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (54868-5979-0)
Product NDC 54868-5979
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name tapentadol hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100319
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name TAPENTADOL HYDROCHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Opioid Agonist [EPC],Opioid Agonists [MoA]

Complete Information of Nucynta


General Information