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 |