Product NDC: | 76329-3352 |
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 |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 76329-3352 |
Labeler Name: | International Medication Systems, Limited |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20000601 |
Package NDC: | 76329-3352-1 |
Package Description: | 1 SYRINGE in 1 CARTON (76329-3352-1) > 50 mL in 1 SYRINGE |
NDC Code | 76329-3352-1 |
Proprietary Name | Sodium Bicarbonate |
Package Description | 1 SYRINGE in 1 CARTON (76329-3352-1) > 50 mL in 1 SYRINGE |
Product NDC | 76329-3352 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Sodium Bicarbonate |
Dosage Form Name | INJECTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20000601 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | International Medication Systems, Limited |
Substance Name | SODIUM BICARBONATE |
Strength Number | 84 |
Strength Unit | mg/mL |
Pharmaceutical Classes |