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Sodium Bicarbonate
Sodium Bicarbonate - 0548-3352-00 - (Sodium Bicarbonate)
Drug Information of Sodium Bicarbonate
| Product NDC: | 0548-3352 |
| Proprietary Name: | Sodium Bicarbonate |
| Non Proprietary Name: | Sodium Bicarbonate |
| Active Ingredient(s): | 84 mg/mL & nbsp; Sodium Bicarbonate |
| Administration Route(s): | PARENTERAL |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sodium Bicarbonate
| Product NDC: | 0548-3352 |
| Labeler Name: | Amphastar Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20000601 |
Package Information of Sodium Bicarbonate
| Package NDC: | 0548-3352-00 |
| Package Description: | 10 SYRINGE in 1 CARTON (0548-3352-00) > 50 mL in 1 SYRINGE |
NDC Information of Sodium Bicarbonate
| NDC Code | 0548-3352-00 |
| Proprietary Name | Sodium Bicarbonate |
| Package Description | 10 SYRINGE in 1 CARTON (0548-3352-00) > 50 mL in 1 SYRINGE |
| Product NDC | 0548-3352 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sodium Bicarbonate |
| Dosage Form Name | INJECTION |
| Route Name | PARENTERAL |
| Start Marketing Date | 20000601 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Amphastar Pharmaceuticals, Inc. |
| Substance Name | SODIUM BICARBONATE |
| Strength Number | 84 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
