| Product ID | 69367-322_6743133a-6d2b-4caf-8809-1a7d225c58d5 |
| NDC | 69367-322 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Potassium Citrate, Sodium Citrate, and Citric Acid |
| Generic Name | Potassium Citrate, Sodium Citrate, And Citric Acid Monohydrate |
| Dosage Form | Solution |
| Route of Administration | ORAL |
| Marketing Start Date | 2021-07-21 |
| Marketing Category | UNAPPROVED DRUG OTHER / |
| Labeler Name | Westminster Pharmaceuticals, LLC |
| Substance Name | POTASSIUM CITRATE; SODIUM CITRATE, UNSPECIFIED FORM; CITRIC ACID MONOHYDRATE |
| Active Ingredient Strength | 550 mg/5mL; mg/5mL; mg/5mL |
| Pharm 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],Acidifying Activity [MoA],Calculi Dissolution Agent [EPC],Anti-coagulant [EPC],Decreased Coagulation Factor Activity [PE],Calcium Chelating Activity [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2022-12-31 |