Product NDC: | 0024-2792 |
Proprietary Name: | Ferrlecit |
Non Proprietary Name: | sodium ferric gluconate complex |
Active Ingredient(s): | 12.5 mg/mL & nbsp; sodium ferric gluconate complex |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0024-2792 |
Labeler Name: | sanofi-aventis U.S. LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020955 |
Marketing Category: | NDA |
Start Marketing Date: | 20110301 |
Package NDC: | 0024-2792-10 |
Package Description: | 10 VIAL, SINGLE-USE in 1 CARTON (0024-2792-10) > 5 mL in 1 VIAL, SINGLE-USE |
NDC Code | 0024-2792-10 |
Proprietary Name | Ferrlecit |
Package Description | 10 VIAL, SINGLE-USE in 1 CARTON (0024-2792-10) > 5 mL in 1 VIAL, SINGLE-USE |
Product NDC | 0024-2792 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | sodium ferric gluconate complex |
Dosage Form Name | INJECTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20110301 |
Marketing Category Name | NDA |
Labeler Name | sanofi-aventis U.S. LLC |
Substance Name | SODIUM FERRIC GLUCONATE COMPLEX |
Strength Number | 12.5 |
Strength Unit | mg/mL |
Pharmaceutical Classes |