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Sodium Bicarbonate
Sodium Bicarbonate - 63739-460-05 - (Sodium Bicarbonate)
Drug Information of Sodium Bicarbonate
| Product NDC: | 63739-460 |
| 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, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sodium Bicarbonate
| Product NDC: | 63739-460 |
| Labeler Name: | McKesson Packaging Services Business Unit of McKesson Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA077394 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100503 |
Package Information of Sodium Bicarbonate
| Package NDC: | 63739-460-05 |
| Package Description: | 5 POUCH in 1 BOX (63739-460-05) > 1 CARTON in 1 POUCH (63739-460-21) > 1 SYRINGE, GLASS in 1 CARTON > 50 mL in 1 SYRINGE, GLASS |
NDC Information of Sodium Bicarbonate
| NDC Code | 63739-460-05 |
| Proprietary Name | Sodium Bicarbonate |
| Package Description | 5 POUCH in 1 BOX (63739-460-05) > 1 CARTON in 1 POUCH (63739-460-21) > 1 SYRINGE, GLASS in 1 CARTON > 50 mL in 1 SYRINGE, GLASS |
| Product NDC | 63739-460 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sodium Bicarbonate |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20100503 |
| Marketing Category Name | NDA |
| Labeler Name | McKesson Packaging Services Business Unit of McKesson Corporation |
| Substance Name | SODIUM BICARBONATE |
| Strength Number | 84 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
