Product NDC: | 0409-6609 |
Proprietary Name: | Neut Sodium Bicarbonate |
Non Proprietary Name: | SODIUM BICARBONATE |
Active Ingredient(s): | .2 g/5mL & nbsp; SODIUM BICARBONATE |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0409-6609 |
Labeler Name: | Hospira, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20050822 |
Package NDC: | 0409-6609-02 |
Package Description: | 25 VIAL in 1 TRAY (0409-6609-02) > 5 mL in 1 VIAL |
NDC Code | 0409-6609-02 |
Proprietary Name | Neut Sodium Bicarbonate |
Package Description | 25 VIAL in 1 TRAY (0409-6609-02) > 5 mL in 1 VIAL |
Product NDC | 0409-6609 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | SODIUM BICARBONATE |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20050822 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Hospira, Inc. |
Substance Name | SODIUM BICARBONATE |
Strength Number | .2 |
Strength Unit | g/5mL |
Pharmaceutical Classes |