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Caldolor
Caldolor - 66220-287-08 - (ibuprofen)
Drug Information of Caldolor
| Product NDC: | 66220-287 |
| 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: | 66220-287 |
| 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: | 66220-287-08 |
| Package Description: | 25 VIAL in 1 CARTON (66220-287-08) > 8 mL in 1 VIAL |
NDC Information of Caldolor
| NDC Code | 66220-287-08 |
| Proprietary Name | Caldolor |
| Package Description | 25 VIAL in 1 CARTON (66220-287-08) > 8 mL in 1 VIAL |
| Product NDC | 66220-287 |
| 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] |
