| Product NDC: | 43825-102 |
| Proprietary Name: | Ofirmev |
| Non Proprietary Name: | acetaminophen |
| Active Ingredient(s): | 10 mg/mL & nbsp; acetaminophen |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 43825-102 |
| Labeler Name: | Cadence Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022450 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20101108 |
| Package NDC: | 43825-102-01 |
| Package Description: | 24 VIAL, GLASS in 1 CARTON (43825-102-01) > 100 mL in 1 VIAL, GLASS |
| NDC Code | 43825-102-01 |
| Proprietary Name | Ofirmev |
| Package Description | 24 VIAL, GLASS in 1 CARTON (43825-102-01) > 100 mL in 1 VIAL, GLASS |
| Product NDC | 43825-102 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | acetaminophen |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20101108 |
| Marketing Category Name | NDA |
| Labeler Name | Cadence Pharmaceuticals, Inc. |
| Substance Name | ACETAMINOPHEN |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |