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Dextrose
Dextrose - 0338-0551-18 - (Dextrose)
Drug Information of Dextrose
| Product NDC: | 0338-0551 |
| Proprietary Name: | Dextrose |
| Non Proprietary Name: | Dextrose |
| Active Ingredient(s): | 5 g/100mL & nbsp; Dextrose |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dextrose
| Product NDC: | 0338-0551 |
| Labeler Name: | BAXTER HEALTHCARE CORPORATION |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA020179 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19921207 |
Package Information of Dextrose
| Package NDC: | 0338-0551-18 |
| Package Description: | 100 mL in 1 BAG (0338-0551-18) |
NDC Information of Dextrose
| NDC Code | 0338-0551-18 |
| Proprietary Name | Dextrose |
| Package Description | 100 mL in 1 BAG (0338-0551-18) |
| Product NDC | 0338-0551 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Dextrose |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19921207 |
| Marketing Category Name | ANDA |
| Labeler Name | BAXTER HEALTHCARE CORPORATION |
| Substance Name | DEXTROSE |
| Strength Number | 5 |
| Strength Unit | g/100mL |
| Pharmaceutical Classes |
