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