Anticoagulant Sodium Citrate is a Extracorporeal Solution in the Human Prescription Drug category. It is labeled and distributed by Laboratorios Grifols Sa. The primary component is Trisodium Citrate Dihydrate.
| Product ID | 76297-006_045bd9a4-99fa-43cd-b712-2efdd04ed22f |
| NDC | 76297-006 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Anticoagulant Sodium Citrate |
| Generic Name | Trisodium Citrate Dihydrate |
| Dosage Form | Solution |
| Route of Administration | EXTRACORPOREAL |
| Marketing Start Date | 2019-10-25 |
| Marketing Category | ANDA / ANDA |
| Application Number | BA125697 |
| Labeler Name | LABORATORIOS GRIFOLS SA |
| Substance Name | TRISODIUM CITRATE DIHYDRATE |
| Active Ingredient Strength | 40 mg/mL |
| Pharm Classes | 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 | 2020-12-31 |
| Marketing Start Date | 2019-10-25 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | BA125697 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2019-10-25 |
| Marketing Category | ANDA |
| Application Number | BA125697 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2019-10-25 |
| Ingredient | Strength |
|---|---|
| TRISODIUM CITRATE DIHYDRATE | 40 mg/mL |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 62646-798 | Anticoagulant Sodium Citrate | Sodium Citrate |
| 76297-006 | Anticoagulant Sodium Citrate | Trisodium Citrate Dihydrate |
| 81839-782 | Anticoagulant Sodium Citrate | Trisodium Citrate Dihydrate |
| 57826-420 | Haemonetics Anticoagulant Sodium Citrate | TRISODIUM CITRATE DIHYDRATE |
| 14537-881 | Sodium Citrate 4% w/v Anticoagulant | TRISODIUM CITRATE DIHYDRATE |
| 14537-883 | Sodium Citrate w/v Anticoagulant | TRISODIUM CITRATE DIHYDRATE |
| 23731-6030 | triCitrasol | Trisodium Citrate dihydrate |