ULTRAM ER - 21695-292-30 - (tramadol hydrochloride)

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Drug Information of ULTRAM ER

Product NDC: 21695-292
Proprietary Name: ULTRAM ER
Non Proprietary Name: tramadol hydrochloride
Active Ingredient(s): 100    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: 21695-292
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021692
Marketing Category: NDA
Start Marketing Date: 20050908

Package Information of ULTRAM ER

Package NDC: 21695-292-30
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (21695-292-30)

NDC Information of ULTRAM ER

NDC Code 21695-292-30
Proprietary Name ULTRAM ER
Package Description 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (21695-292-30)
Product NDC 21695-292
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name tramadol hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20050908
Marketing Category Name NDA
Labeler Name Rebel Distributors Corp
Substance Name TRAMADOL HYDROCHLORIDE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of ULTRAM ER


General Information