ULTRAM - 55289-650-15 - (tramadol hydrochloride)

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Drug Information of ULTRAM

Product NDC: 55289-650
Proprietary Name: ULTRAM
Non Proprietary Name: tramadol hydrochloride
Active Ingredient(s): 50    mg/1 & nbsp;   tramadol hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of ULTRAM

Product NDC: 55289-650
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020281
Marketing Category: NDA
Start Marketing Date: 19950303

Package Information of ULTRAM

Package NDC: 55289-650-15
Package Description: 15 TABLET, COATED in 1 BOTTLE, PLASTIC (55289-650-15)

NDC Information of ULTRAM

NDC Code 55289-650-15
Proprietary Name ULTRAM
Package Description 15 TABLET, COATED in 1 BOTTLE, PLASTIC (55289-650-15)
Product NDC 55289-650
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name tramadol hydrochloride
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 19950303
Marketing Category Name NDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name TRAMADOL HYDROCHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of ULTRAM


General Information