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Dextrose
Dextrose - 0338-0711-34 - (Dextrose Monohydrate)
Drug Information of Dextrose
| Product NDC: | 0338-0711 |
| Proprietary Name: | Dextrose |
| Non Proprietary Name: | Dextrose Monohydrate |
| Active Ingredient(s): | 20 g/100mL & nbsp; Dextrose Monohydrate |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dextrose
| Product NDC: | 0338-0711 |
| Labeler Name: | Baxter Healthcare Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA017521 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19790828 |
Package Information of Dextrose
| Package NDC: | 0338-0711-34 |
| Package Description: | 1000 mL in 1 BAG (0338-0711-34) |
NDC Information of Dextrose
| NDC Code | 0338-0711-34 |
| Proprietary Name | Dextrose |
| Package Description | 1000 mL in 1 BAG (0338-0711-34) |
| Product NDC | 0338-0711 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Dextrose Monohydrate |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19790828 |
| Marketing Category Name | NDA |
| Labeler Name | Baxter Healthcare Company |
| Substance Name | DEXTROSE MONOHYDRATE |
| Strength Number | 20 |
| Strength Unit | g/100mL |
| Pharmaceutical Classes |
