Vicoprofen - 54868-4035-3 - (Hydrocodone Bitartrate and Ibuprofen)

Alphabetical Index


Drug Information of Vicoprofen

Product NDC: 54868-4035
Proprietary Name: Vicoprofen
Non Proprietary Name: Hydrocodone Bitartrate and Ibuprofen
Active Ingredient(s): 7.5; 200    mg/1; mg/1 & nbsp;   Hydrocodone Bitartrate and Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Vicoprofen

Product NDC: 54868-4035
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020716
Marketing Category: NDA
Start Marketing Date: 19980513

Package Information of Vicoprofen

Package NDC: 54868-4035-3
Package Description: 15 TABLET, COATED in 1 BOTTLE (54868-4035-3)

NDC Information of Vicoprofen

NDC Code 54868-4035-3
Proprietary Name Vicoprofen
Package Description 15 TABLET, COATED in 1 BOTTLE (54868-4035-3)
Product NDC 54868-4035
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrocodone Bitartrate and Ibuprofen
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 19980513
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name HYDROCODONE BITARTRATE; IBUPROFEN
Strength Number 7.5; 200
Strength Unit mg/1; mg/1
Pharmaceutical Classes Opioid Agonist [EPC],Opioid Agonists [MoA],Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of Vicoprofen


General Information