Rybix - 68453-825-09 - (tramadol hydrochloride)

Alphabetical Index


Drug Information of Rybix

Product NDC: 68453-825
Proprietary Name: Rybix
Non Proprietary Name: tramadol hydrochloride
Active Ingredient(s): 50    mg/1 & nbsp;   tramadol hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, ORALLY DISINTEGRATING
Coding System: National Drug Codes(NDC)

Labeler Information of Rybix

Product NDC: 68453-825
Labeler Name: Victory Pharma, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021693
Marketing Category: NDA
Start Marketing Date: 20100501

Package Information of Rybix

Package NDC: 68453-825-09
Package Description: 15 BLISTER PACK in 1 CARTON (68453-825-09) > 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

NDC Information of Rybix

NDC Code 68453-825-09
Proprietary Name Rybix
Package Description 15 BLISTER PACK in 1 CARTON (68453-825-09) > 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Product NDC 68453-825
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name tramadol hydrochloride
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20100501
Marketing Category Name NDA
Labeler Name Victory Pharma, Inc.
Substance Name TRAMADOL HYDROCHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Rybix


General Information