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DEXTROSE
DEXTROSE - 0264-7520-20 - (DEXTROSE)
Drug Information of DEXTROSE
| Product NDC: | 0264-7520 |
| Proprietary Name: | DEXTROSE |
| Non Proprietary Name: | DEXTROSE |
| Active Ingredient(s): | 10 g/100mL & nbsp; DEXTROSE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DEXTROSE
| Product NDC: | 0264-7520 |
| Labeler Name: | B. Braun Medical Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019626 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19880202 |
Package Information of DEXTROSE
| Package NDC: | 0264-7520-20 |
| Package Description: | 24 CONTAINER in 1 CASE (0264-7520-20) > 250 mL in 1 CONTAINER |
NDC Information of DEXTROSE
| NDC Code | 0264-7520-20 |
| Proprietary Name | DEXTROSE |
| Package Description | 24 CONTAINER in 1 CASE (0264-7520-20) > 250 mL in 1 CONTAINER |
| Product NDC | 0264-7520 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | DEXTROSE |
| Dosage Form Name | SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19880202 |
| Marketing Category Name | NDA |
| Labeler Name | B. Braun Medical Inc. |
| Substance Name | DEXTROSE |
| Strength Number | 10 |
| Strength Unit | g/100mL |
| Pharmaceutical Classes |
