Product NDC: | 0409-6637 |
Proprietary Name: | Sodium Bicarbonate |
Non Proprietary Name: | SODIUM BICARBONATE |
Active Ingredient(s): | 84 mg/mL & nbsp; SODIUM BICARBONATE |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0409-6637 |
Labeler Name: | Hospira, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 19840413 |
Package NDC: | 0409-6637-34 |
Package Description: | 50 mL in 1 SYRINGE (0409-6637-34) |
NDC Code | 0409-6637-34 |
Proprietary Name | Sodium Bicarbonate |
Package Description | 50 mL in 1 SYRINGE (0409-6637-34) |
Product NDC | 0409-6637 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | SODIUM BICARBONATE |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 19840413 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Hospira, Inc. |
Substance Name | SODIUM BICARBONATE |
Strength Number | 84 |
Strength Unit | mg/mL |
Pharmaceutical Classes |