Product NDC: | 52533-095 |
Proprietary Name: | Dextrose |
Non Proprietary Name: | Dextrose Monohydrate Injection, Solution |
Active Ingredient(s): | 25 mg/mL & nbsp; Dextrose Monohydrate Injection, Solution |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52533-095 |
Labeler Name: | Cantrell Drug Company |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20110218 |
Package NDC: | 52533-095-24 |
Package Description: | 1000 mL in 1 BAG (52533-095-24) |
NDC Code | 52533-095-24 |
Proprietary Name | Dextrose |
Package Description | 1000 mL in 1 BAG (52533-095-24) |
Product NDC | 52533-095 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Dextrose Monohydrate Injection, Solution |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20110218 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Cantrell Drug Company |
Substance Name | DEXTROSE MONOHYDRATE |
Strength Number | 25 |
Strength Unit | mg/mL |
Pharmaceutical Classes |