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Sodium Citrate and Citric Acid
Sodium Citrate and Citric Acid - 55154-9419-5 - (SODIUM CITRATE and CITRIC ACID MONOHYDRATE)
Drug Information of Sodium Citrate and Citric Acid
| Product NDC: | 55154-9419 |
| Proprietary Name: | Sodium Citrate and Citric Acid |
| Non Proprietary Name: | SODIUM CITRATE and CITRIC ACID MONOHYDRATE |
| Active Ingredient(s): | 334; 500 mg/5mL; mg/5mL & nbsp; SODIUM CITRATE and CITRIC ACID MONOHYDRATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sodium Citrate and Citric Acid
| Product NDC: | 55154-9419 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19690101 |
Package Information of Sodium Citrate and Citric Acid
| Package NDC: | 55154-9419-5 |
| Package Description: | 5 CUP, UNIT-DOSE in 1 BAG (55154-9419-5) > 15 mL in 1 CUP, UNIT-DOSE |
NDC Information of Sodium Citrate and Citric Acid
| NDC Code | 55154-9419-5 |
| Proprietary Name | Sodium Citrate and Citric Acid |
| Package Description | 5 CUP, UNIT-DOSE in 1 BAG (55154-9419-5) > 15 mL in 1 CUP, UNIT-DOSE |
| Product NDC | 55154-9419 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SODIUM CITRATE and CITRIC ACID MONOHYDRATE |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 19690101 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Cardinal Health |
| Substance Name | CITRIC ACID MONOHYDRATE; SODIUM CITRATE |
| Strength Number | 334; 500 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes | Acidifying Activity [MoA],Calculi Dissolution Agent [EPC],Anti-coagulant [EPC],Decreased Coagulation Factor Activity [PE],Calcium Chelating Activity [MoA],Acidifying Activity [MoA],Calculi Dissolution Agent [EPC],Anti-coagulant [EPC],Decreased Coagulation Factor Activity [PE],Calcium Chelating Activity [MoA] |
