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Sodium Bicarbonate
Sodium Bicarbonate - 0409-3486-16 - (SODIUM BICARBONATE)
Drug Information of Sodium Bicarbonate
| Product NDC: | 0409-3486 |
| Proprietary Name: | Sodium Bicarbonate |
| Non Proprietary Name: | SODIUM BICARBONATE |
| Active Ingredient(s): | 75 mg/mL & nbsp; SODIUM BICARBONATE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sodium Bicarbonate
| Product NDC: | 0409-3486 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077394 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120418 |
Package Information of Sodium Bicarbonate
| Package NDC: | 0409-3486-16 |
| Package Description: | 10 CARTON in 1 CONTAINER (0409-3486-16) > 1 SYRINGE, PLASTIC in 1 CARTON > 50 mL in 1 SYRINGE, PLASTIC |
NDC Information of Sodium Bicarbonate
| NDC Code | 0409-3486-16 |
| Proprietary Name | Sodium Bicarbonate |
| Package Description | 10 CARTON in 1 CONTAINER (0409-3486-16) > 1 SYRINGE, PLASTIC in 1 CARTON > 50 mL in 1 SYRINGE, PLASTIC |
| Product NDC | 0409-3486 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SODIUM BICARBONATE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20120418 |
| Marketing Category Name | ANDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | SODIUM BICARBONATE |
| Strength Number | 75 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
