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DEXTROSE
DEXTROSE - 0338-0017-41 - (DEXTROSE MONOHYDRATE)
Drug Information of DEXTROSE
| Product NDC: | 0338-0017 |
| Proprietary Name: | DEXTROSE |
| Non Proprietary Name: | DEXTROSE MONOHYDRATE |
| Active Ingredient(s): | 50 g/1000mL & nbsp; DEXTROSE MONOHYDRATE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DEXTROSE
| Product NDC: | 0338-0017 |
| Labeler Name: | Baxter Healthcare Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA016673 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100616 |
Package Information of DEXTROSE
| Package NDC: | 0338-0017-41 |
| Package Description: | 1 BAG in 1 PACKAGE (0338-0017-41) > 50 mL in 1 BAG |
NDC Information of DEXTROSE
| NDC Code | 0338-0017-41 |
| Proprietary Name | DEXTROSE |
| Package Description | 1 BAG in 1 PACKAGE (0338-0017-41) > 50 mL in 1 BAG |
| Product NDC | 0338-0017 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | DEXTROSE MONOHYDRATE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20100616 |
| Marketing Category Name | ANDA |
| Labeler Name | Baxter Healthcare Corporation |
| Substance Name | DEXTROSE MONOHYDRATE |
| Strength Number | 50 |
| Strength Unit | g/1000mL |
| Pharmaceutical Classes |
