| 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 |