ULTRACET - 54868-4703-1 - (tramadol hydrochloride and acetaminophen)

Alphabetical Index


Drug Information of ULTRACET

Product NDC: 54868-4703
Proprietary Name: ULTRACET
Non Proprietary Name: tramadol hydrochloride and acetaminophen
Active Ingredient(s): 325; 37.5    mg/1; mg/1 & nbsp;   tramadol hydrochloride and acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of ULTRACET

Product NDC: 54868-4703
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021123
Marketing Category: NDA
Start Marketing Date: 20021030

Package Information of ULTRACET

Package NDC: 54868-4703-1
Package Description: 10 TABLET, COATED in 1 BOTTLE (54868-4703-1)

NDC Information of ULTRACET

NDC Code 54868-4703-1
Proprietary Name ULTRACET
Package Description 10 TABLET, COATED in 1 BOTTLE (54868-4703-1)
Product NDC 54868-4703
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name tramadol hydrochloride and acetaminophen
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20021030
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE
Strength Number 325; 37.5
Strength Unit mg/1; mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of ULTRACET


General Information