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Sodium Bicarbonate
Sodium Bicarbonate - 50509-100-04 - (Sodium Bicarbonate)
Drug Information of Sodium Bicarbonate
| Product NDC: | 50509-100 |
| Proprietary Name: | Sodium Bicarbonate |
| Non Proprietary Name: | Sodium Bicarbonate |
| Active Ingredient(s): | 1 meq/mL & nbsp; Sodium Bicarbonate |
| Administration Route(s): | PARENTERAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sodium Bicarbonate
| Product NDC: | 50509-100 |
| Labeler Name: | Onpharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100722 |
Package Information of Sodium Bicarbonate
| Package NDC: | 50509-100-04 |
| Package Description: | 4 CARTRIDGE in 1 CARTON (50509-100-04) > 1.7 mL in 1 CARTRIDGE (50509-100-03) |
NDC Information of Sodium Bicarbonate
| NDC Code | 50509-100-04 |
| Proprietary Name | Sodium Bicarbonate |
| Package Description | 4 CARTRIDGE in 1 CARTON (50509-100-04) > 1.7 mL in 1 CARTRIDGE (50509-100-03) |
| Product NDC | 50509-100 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sodium Bicarbonate |
| Dosage Form Name | SOLUTION |
| Route Name | PARENTERAL |
| Start Marketing Date | 20100722 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Onpharma, Inc. |
| Substance Name | SODIUM BICARBONATE |
| Strength Number | 1 |
| Strength Unit | meq/mL |
| Pharmaceutical Classes |
