Product NDC: | 0409-7923 |
Proprietary Name: | Dextrose |
Non Proprietary Name: | DEXTROSE MONOHYDRATE |
Active Ingredient(s): | 5 g/100mL & nbsp; DEXTROSE MONOHYDRATE |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0409-7923 |
Labeler Name: | Hospira, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA016367 |
Marketing Category: | NDA |
Start Marketing Date: | 20100223 |
Package NDC: | 0409-7923-13 |
Package Description: | 48 BAG in 1 CASE (0409-7923-13) > 50 mL in 1 BAG |
NDC Code | 0409-7923-13 |
Proprietary Name | Dextrose |
Package Description | 48 BAG in 1 CASE (0409-7923-13) > 50 mL in 1 BAG |
Product NDC | 0409-7923 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | DEXTROSE MONOHYDRATE |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20100223 |
Marketing Category Name | NDA |
Labeler Name | Hospira, Inc. |
Substance Name | DEXTROSE MONOHYDRATE |
Strength Number | 5 |
Strength Unit | g/100mL |
Pharmaceutical Classes |