Product NDC: | 52584-625 |
Proprietary Name: | Sodium Bicarbonate |
Non Proprietary Name: | Sodium Bicarbonate |
Active Ingredient(s): | 1 meq/mL & nbsp; Sodium Bicarbonate |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52584-625 |
Labeler Name: | General Injectables & Vaccines, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20100801 |
Package NDC: | 52584-625-02 |
Package Description: | 1 VIAL, SINGLE-DOSE in 1 BAG (52584-625-02) > 50 mL in 1 VIAL, SINGLE-DOSE |
NDC Code | 52584-625-02 |
Proprietary Name | Sodium Bicarbonate |
Package Description | 1 VIAL, SINGLE-DOSE in 1 BAG (52584-625-02) > 50 mL in 1 VIAL, SINGLE-DOSE |
Product NDC | 52584-625 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Sodium Bicarbonate |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20100801 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | General Injectables & Vaccines, Inc |
Substance Name | SODIUM BICARBONATE |
Strength Number | 1 |
Strength Unit | meq/mL |
Pharmaceutical Classes |