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Haemonetics Anticoagulant Sodium Citrate
Haemonetics Anticoagulant Sodium Citrate - 57826-420-02 - (TRISODIUM CITRATE DIHYDRATE)
Drug Information of Haemonetics Anticoagulant Sodium Citrate
| Product NDC: | 57826-420 |
| Proprietary Name: | Haemonetics Anticoagulant Sodium Citrate |
| Non Proprietary Name: | TRISODIUM CITRATE DIHYDRATE |
| Active Ingredient(s): | 40 mg/mL & nbsp; TRISODIUM CITRATE DIHYDRATE |
| Administration Route(s): | EXTRACORPOREAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Haemonetics Anticoagulant Sodium Citrate
| Product NDC: | 57826-420 |
| Labeler Name: | Haemonetics Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | BLA980123 |
| Marketing Category: | BLA |
| Start Marketing Date: | 20130110 |
Package Information of Haemonetics Anticoagulant Sodium Citrate
| Package NDC: | 57826-420-02 |
| Package Description: | 250 mL in 1 BAG (57826-420-02) |
NDC Information of Haemonetics Anticoagulant Sodium Citrate
| NDC Code | 57826-420-02 |
| Proprietary Name | Haemonetics Anticoagulant Sodium Citrate |
| Package Description | 250 mL in 1 BAG (57826-420-02) |
| Product NDC | 57826-420 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | TRISODIUM CITRATE DIHYDRATE |
| Dosage Form Name | SOLUTION |
| Route Name | EXTRACORPOREAL |
| Start Marketing Date | 20130110 |
| Marketing Category Name | BLA |
| Labeler Name | Haemonetics Corporation |
| Substance Name | TRISODIUM CITRATE DIHYDRATE |
| Strength Number | 40 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Acidifying Activity [MoA],Calculi Dissolution Agent [EPC],Anti-coagulant [EPC],Decreased Coagulation Factor Activity [PE],Calcium Chelating Activity [MoA] |
