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Sodium Chloride
Sodium Chloride - 0338-0049-31 - (Sodium Chloride)
Drug Information of Sodium Chloride
| Product NDC: | 0338-0049 |
| Proprietary Name: | Sodium Chloride |
| Non Proprietary Name: | Sodium Chloride |
| Active Ingredient(s): | 9 g/1000mL & nbsp; Sodium Chloride |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sodium Chloride
| Product NDC: | 0338-0049 |
| Labeler Name: | Baxter Healthcare Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA016677 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19701209 |
Package Information of Sodium Chloride
| Package NDC: | 0338-0049-31 |
| Package Description: | 16 BAG in 1 PACKAGE (0338-0049-31) > 50 mL in 1 BAG |
NDC Information of Sodium Chloride
| NDC Code | 0338-0049-31 |
| Proprietary Name | Sodium Chloride |
| Package Description | 16 BAG in 1 PACKAGE (0338-0049-31) > 50 mL in 1 BAG |
| Product NDC | 0338-0049 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sodium Chloride |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19701209 |
| Marketing Category Name | NDA |
| Labeler Name | Baxter Healthcare Corporation |
| Substance Name | SODIUM CHLORIDE |
| Strength Number | 9 |
| Strength Unit | g/1000mL |
| Pharmaceutical Classes |
