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Dextrose
Dextrose - 0409-6648-02 - (DEXTROSE MONOHYDRATE)
Drug Information of Dextrose
| Product NDC: | 0409-6648 |
| Proprietary Name: | Dextrose |
| Non Proprietary Name: | DEXTROSE MONOHYDRATE |
| Active Ingredient(s): | 25 g/50mL & nbsp; DEXTROSE MONOHYDRATE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dextrose
| Product NDC: | 0409-6648 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019445 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110629 |
Package Information of Dextrose
| Package NDC: | 0409-6648-02 |
| Package Description: | 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-6648-02) > 50 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Dextrose
| NDC Code | 0409-6648-02 |
| Proprietary Name | Dextrose |
| Package Description | 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-6648-02) > 50 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 0409-6648 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | DEXTROSE MONOHYDRATE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20110629 |
| Marketing Category Name | NDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | DEXTROSE MONOHYDRATE |
| Strength Number | 25 |
| Strength Unit | g/50mL |
| Pharmaceutical Classes |
