Ultram - 49349-845-03 - (Tramadol Hydrochloride)

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Drug Information of Ultram

Product NDC: 49349-845
Proprietary Name: Ultram
Non Proprietary Name: Tramadol Hydrochloride
Active Ingredient(s): 100    mg/1 & nbsp;   Tramadol Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Ultram

Product NDC: 49349-845
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021692
Marketing Category: NDA
Start Marketing Date: 20120301

Package Information of Ultram

Package NDC: 49349-845-03
Package Description: 20 TABLET in 1 VIAL (49349-845-03)

NDC Information of Ultram

NDC Code 49349-845-03
Proprietary Name Ultram
Package Description 20 TABLET in 1 VIAL (49349-845-03)
Product NDC 49349-845
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tramadol Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120301
Marketing Category Name NDA
Labeler Name REMEDYREPACK INC.
Substance Name TRAMADOL HYDROCHLORIDE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Ultram


General Information