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Dextrose and Sodium Chloride
Dextrose and Sodium Chloride - 0338-6308-03 - (dextrose monohydrate and sodium chloride)
Drug Information of Dextrose and Sodium Chloride
| Product NDC: | 0338-6308 |
| Proprietary Name: | Dextrose and Sodium Chloride |
| Non Proprietary Name: | dextrose monohydrate and sodium chloride |
| Active Ingredient(s): | 5; 450 g/100mL; mg/100mL & nbsp; dextrose monohydrate and sodium chloride |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dextrose and Sodium Chloride
| Product NDC: | 0338-6308 |
| Labeler Name: | Baxter Healthcare Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA016683 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19710322 |
Package Information of Dextrose and Sodium Chloride
| Package NDC: | 0338-6308-03 |
| Package Description: | 500 mL in 1 BAG (0338-6308-03) |
NDC Information of Dextrose and Sodium Chloride
| NDC Code | 0338-6308-03 |
| Proprietary Name | Dextrose and Sodium Chloride |
| Package Description | 500 mL in 1 BAG (0338-6308-03) |
| Product NDC | 0338-6308 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | dextrose monohydrate and sodium chloride |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19710322 |
| Marketing Category Name | NDA |
| Labeler Name | Baxter Healthcare Corporation |
| Substance Name | DEXTROSE MONOHYDRATE; SODIUM CHLORIDE |
| Strength Number | 5; 450 |
| Strength Unit | g/100mL; mg/100mL |
| Pharmaceutical Classes |
