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Nulecit
Nulecit - 52544-149-87 - (sodium ferric gluconate complex)
Drug Information of Nulecit
| Product NDC: | 52544-149 |
| Proprietary Name: | Nulecit |
| 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) |
Labeler Information of Nulecit
| Product NDC: | 52544-149 |
| Labeler Name: | Watson Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078215 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110331 |
Package Information of Nulecit
| Package NDC: | 52544-149-87 |
| Package Description: | 10 VIAL in 1 CARTON (52544-149-87) > 5 mL in 1 VIAL |
NDC Information of Nulecit
| NDC Code | 52544-149-87 |
| Proprietary Name | Nulecit |
| Package Description | 10 VIAL in 1 CARTON (52544-149-87) > 5 mL in 1 VIAL |
| Product NDC | 52544-149 |
| 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 Pharma, Inc. |
| Substance Name | SODIUM FERRIC GLUCONATE COMPLEX |
| Strength Number | 12.5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
