NUCYNTA - 16590-889-30 - (TAPENTADOL HYDROCHLORIDE)

Alphabetical Index


Drug Information of NUCYNTA

Product NDC: 16590-889
Proprietary Name: NUCYNTA
Non Proprietary Name: TAPENTADOL HYDROCHLORIDE
Active Ingredient(s): 75    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: 16590-889
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022304
Marketing Category: NDA
Start Marketing Date: 20090601

Package Information of NUCYNTA

Package NDC: 16590-889-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (16590-889-30)

NDC Information of NUCYNTA

NDC Code 16590-889-30
Proprietary Name NUCYNTA
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (16590-889-30)
Product NDC 16590-889
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name TAPENTADOL HYDROCHLORIDE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20090601
Marketing Category Name NDA
Labeler Name STAT RX USA LLC
Substance Name TAPENTADOL HYDROCHLORIDE
Strength Number 75
Strength Unit mg/1
Pharmaceutical Classes Opioid Agonist [EPC],Opioid Agonists [MoA]

Complete Information of NUCYNTA


General Information