RYZOLT - 59011-335-60 - (TRAMADOL HYDROCHLORIDE)

Alphabetical Index


Drug Information of RYZOLT

Product NDC: 59011-335
Proprietary Name: RYZOLT
Non Proprietary Name: TRAMADOL HYDROCHLORIDE
Active Ingredient(s): 200    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: 59011-335
Labeler Name: Purdue Pharma LP
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021745
Marketing Category: NDA
Start Marketing Date: 20081215

Package Information of RYZOLT

Package NDC: 59011-335-60
Package Description: 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (59011-335-60)

NDC Information of RYZOLT

NDC Code 59011-335-60
Proprietary Name RYZOLT
Package Description 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (59011-335-60)
Product NDC 59011-335
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name TRAMADOL HYDROCHLORIDE
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20081215
Marketing Category Name NDA
Labeler Name Purdue Pharma LP
Substance Name TRAMADOL HYDROCHLORIDE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of RYZOLT


General Information