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 |