Ultram ER - 50458-655-30 - (Tramadol Hydrochloride)

Alphabetical Index


Drug Information of Ultram ER

Product NDC: 50458-655
Proprietary Name: Ultram ER
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 Ultram ER

Product NDC: 50458-655
Labeler Name: Janssen Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021692
Marketing Category: NDA
Start Marketing Date: 20051001

Package Information of Ultram ER

Package NDC: 50458-655-30
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50458-655-30)

NDC Information of Ultram ER

NDC Code 50458-655-30
Proprietary Name Ultram ER
Package Description 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50458-655-30)
Product NDC 50458-655
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tramadol Hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20051001
Marketing Category Name NDA
Labeler Name Janssen Pharmaceuticals, Inc.
Substance Name TRAMADOL HYDROCHLORIDE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Ultram ER


General Information