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Dextrose
Dextrose - 63739-461-05 - (Dextrose)
Drug Information of Dextrose
| Product NDC: | 63739-461 |
| Proprietary Name: | Dextrose |
| Non Proprietary Name: | Dextrose |
| Active Ingredient(s): | 25 g/50mL & nbsp; Dextrose |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dextrose
| Product NDC: | 63739-461 |
| Labeler Name: | McKesson Packaging Services Business Unit of McKesson Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100503 |
Package Information of Dextrose
| Package NDC: | 63739-461-05 |
| Package Description: | 5 POUCH in 1 BOX (63739-461-05) > 1 SYRINGE in 1 POUCH (63739-461-21) > 50 mL in 1 SYRINGE |
NDC Information of Dextrose
| NDC Code | 63739-461-05 |
| Proprietary Name | Dextrose |
| Package Description | 5 POUCH in 1 BOX (63739-461-05) > 1 SYRINGE in 1 POUCH (63739-461-21) > 50 mL in 1 SYRINGE |
| Product NDC | 63739-461 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Dextrose |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20100503 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | McKesson Packaging Services Business Unit of McKesson Corporation |
| Substance Name | DEXTROSE |
| Strength Number | 25 |
| Strength Unit | g/50mL |
| Pharmaceutical Classes |
