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sodium bicarbonate
sodium bicarbonate - 25021-501-66 - (sodium bicarbonate)
Drug Information of sodium bicarbonate
| Product NDC: | 25021-501 |
| 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): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of sodium bicarbonate
| Product NDC: | 25021-501 |
| Labeler Name: | Sagent Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE |
| Start Marketing Date: | 20121002 |
Package Information of sodium bicarbonate
| Package NDC: | 25021-501-66 |
| Package Description: | 10 VIAL in 1 CARTON (25021-501-66) > 10 mL in 1 VIAL |
NDC Information of sodium bicarbonate
| NDC Code | 25021-501-66 |
| Proprietary Name | sodium bicarbonate |
| Package Description | 10 VIAL in 1 CARTON (25021-501-66) > 10 mL in 1 VIAL |
| Product NDC | 25021-501 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | sodium bicarbonate |
| Dosage Form Name | SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20121002 |
| Marketing Category Name | UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE |
| Labeler Name | Sagent Pharmaceuticals |
| Substance Name | SODIUM BICARBONATE |
| Strength Number | 84 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
