RYZOLT - 35356-498-30 - (TRAMADOL HYDROCHLORIDE)

Alphabetical Index


Drug Information of RYZOLT

Product NDC: 35356-498
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: 35356-498
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021745
Marketing Category: NDA
Start Marketing Date: 20120322

Package Information of RYZOLT

Package NDC: 35356-498-30
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (35356-498-30)

NDC Information of RYZOLT

NDC Code 35356-498-30
Proprietary Name RYZOLT
Package Description 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (35356-498-30)
Product NDC 35356-498
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name TRAMADOL HYDROCHLORIDE
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20120322
Marketing Category Name NDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
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