Home
>
National Drug Code (NDC)
>
Sodium Lactate
Sodium Lactate - 0409-6664-02 - (SODIUM LACTATE)
Drug Information of Sodium Lactate
| Product NDC: | 0409-6664 |
| Proprietary Name: | Sodium Lactate |
| Non Proprietary Name: | SODIUM LACTATE |
| Active Ingredient(s): | 5.6 g/10mL & nbsp; SODIUM LACTATE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION, CONCENTRATE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sodium Lactate
| Product NDC: | 0409-6664 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018947 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110816 |
Package Information of Sodium Lactate
| Package NDC: | 0409-6664-02 |
| Package Description: | 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-6664-02) > 10 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Sodium Lactate
| NDC Code | 0409-6664-02 |
| Proprietary Name | Sodium Lactate |
| Package Description | 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-6664-02) > 10 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 0409-6664 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SODIUM LACTATE |
| Dosage Form Name | INJECTION, SOLUTION, CONCENTRATE |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20110816 |
| Marketing Category Name | NDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | SODIUM LACTATE |
| Strength Number | 5.6 |
| Strength Unit | g/10mL |
| Pharmaceutical Classes |
