NeoProfen - 67386-122-52 - (ibuprofen lysine)

Alphabetical Index


Drug Information of NeoProfen

Product NDC: 67386-122
Proprietary Name: NeoProfen
Non Proprietary Name: ibuprofen lysine
Active Ingredient(s): 10    mg/mL & nbsp;   ibuprofen lysine
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of NeoProfen

Product NDC: 67386-122
Labeler Name: Lundbeck Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021903
Marketing Category: NDA
Start Marketing Date: 20060413

Package Information of NeoProfen

Package NDC: 67386-122-52
Package Description: 3 VIAL in 1 CARTON (67386-122-52) > 2 mL in 1 VIAL

NDC Information of NeoProfen

NDC Code 67386-122-52
Proprietary Name NeoProfen
Package Description 3 VIAL in 1 CARTON (67386-122-52) > 2 mL in 1 VIAL
Product NDC 67386-122
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ibuprofen lysine
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20060413
Marketing Category Name NDA
Labeler Name Lundbeck Inc.
Substance Name IBUPROFEN LYSINE
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of NeoProfen


General Information