ULTRACET - 49999-118-30 - (tramadol hydrochloride and acetaminophen)

Alphabetical Index


Drug Information of ULTRACET

Product NDC: 49999-118
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
Coding System: National Drug Codes(NDC)

Labeler Information of ULTRACET

Product NDC: 49999-118
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021123
Marketing Category: NDA
Start Marketing Date: 20120320

Package Information of ULTRACET

Package NDC: 49999-118-30
Package Description: 30 TABLET in 1 BOTTLE (49999-118-30)

NDC Information of ULTRACET

NDC Code 49999-118-30
Proprietary Name ULTRACET
Package Description 30 TABLET in 1 BOTTLE (49999-118-30)
Product NDC 49999-118
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name tramadol hydrochloride and acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120320
Marketing Category Name NDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
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