RYZOLT - 16590-255-60 - (TRAMADOL HYDROCHLORIDE)

Alphabetical Index


Drug Information of RYZOLT

Product NDC: 16590-255
Proprietary Name: RYZOLT
Non Proprietary Name: TRAMADOL HYDROCHLORIDE
Active Ingredient(s): 300    mg/1 & nbsp;   TRAMADOL HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of RYZOLT

Product NDC: 16590-255
Labeler Name: Stat Rx USA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021745
Marketing Category: NDA
Start Marketing Date: 20081230

Package Information of RYZOLT

Package NDC: 16590-255-60
Package Description: 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (16590-255-60)

NDC Information of RYZOLT

NDC Code 16590-255-60
Proprietary Name RYZOLT
Package Description 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (16590-255-60)
Product NDC 16590-255
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name TRAMADOL HYDROCHLORIDE
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20081230
Marketing Category Name NDA
Labeler Name Stat Rx USA
Substance Name TRAMADOL HYDROCHLORIDE
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of RYZOLT


General Information