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Sodium Lactate
Sodium Lactate - 0338-0129-04 - (Sodium Lactate)
Drug Information of Sodium Lactate
| Product NDC: | 0338-0129 |
| Proprietary Name: | Sodium Lactate |
| Non Proprietary Name: | Sodium Lactate |
| Active Ingredient(s): | 1.87 g/100mL & nbsp; Sodium Lactate |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sodium Lactate
| Product NDC: | 0338-0129 |
| Labeler Name: | Baxter Healthcare Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA016692 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20111019 |
Package Information of Sodium Lactate
| Package NDC: | 0338-0129-04 |
| Package Description: | 1000 mL in 1 BAG (0338-0129-04) |
NDC Information of Sodium Lactate
| NDC Code | 0338-0129-04 |
| Proprietary Name | Sodium Lactate |
| Package Description | 1000 mL in 1 BAG (0338-0129-04) |
| Product NDC | 0338-0129 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sodium Lactate |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20111019 |
| Marketing Category Name | NDA |
| Labeler Name | Baxter Healthcare Corporation |
| Substance Name | SODIUM LACTATE |
| Strength Number | 1.87 |
| Strength Unit | g/100mL |
| Pharmaceutical Classes |
