Product ID | 17856-0677_bf4b98cb-eacf-4489-ac73-319e8cb04625 |
NDC | 17856-0677 |
Product Type | Human Prescription Drug |
Proprietary Name | TRICITRATES |
Generic Name | Potassium Citrate, Sodium Citrate, And Citric Acid Monohydrate |
Dosage Form | Solution |
Route of Administration | ORAL |
Marketing Start Date | 2018-08-21 |
Marketing Category | UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER |
Labeler Name | ATLANTIC BIOLOGICALS CORP. |
Substance Name | POTASSIUM CITRATE; SODIUM CITRATE; 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 | 2019-12-31 |