Caldolor - 66220-247-04 - (ibuprofen)

Alphabetical Index


Drug Information of Caldolor

Product NDC: 66220-247
Proprietary Name: Caldolor
Non Proprietary Name: ibuprofen
Active Ingredient(s): 100    mg/mL & nbsp;   ibuprofen
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Caldolor

Product NDC: 66220-247
Labeler Name: Cumberland Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022348
Marketing Category: NDA
Start Marketing Date: 20090827

Package Information of Caldolor

Package NDC: 66220-247-04
Package Description: 25 VIAL in 1 CARTON (66220-247-04) > 4 mL in 1 VIAL

NDC Information of Caldolor

NDC Code 66220-247-04
Proprietary Name Caldolor
Package Description 25 VIAL in 1 CARTON (66220-247-04) > 4 mL in 1 VIAL
Product NDC 66220-247
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ibuprofen
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20090827
Marketing Category Name NDA
Labeler Name Cumberland Pharmaceuticals Inc.
Substance Name IBUPROFEN
Strength Number 100
Strength Unit mg/mL
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of Caldolor


General Information