Product NDC: | 0591-0149 |
Proprietary Name: | Sodium Ferric Gluconate Complex |
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: | 0591-0149 |
Labeler Name: | Watson Laboratories, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA078215 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110331 |
Package NDC: | 0591-0149-87 |
Package Description: | 10 VIAL in 1 CARTON (0591-0149-87) > 5 mL in 1 VIAL (0591-0149-26) |
NDC Code | 0591-0149-87 |
Proprietary Name | Sodium Ferric Gluconate Complex |
Package Description | 10 VIAL in 1 CARTON (0591-0149-87) > 5 mL in 1 VIAL (0591-0149-26) |
Product NDC | 0591-0149 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Sodium Ferric Gluconate Complex |
Dosage Form Name | INJECTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20110331 |
Marketing Category Name | ANDA |
Labeler Name | Watson Laboratories, Inc. |
Substance Name | SODIUM FERRIC GLUCONATE COMPLEX |
Strength Number | 12.5 |
Strength Unit | mg/mL |
Pharmaceutical Classes |