Haemonetics Anticoagulant Sodium Citrate
- Product NDC
- 57826-420
- 11-digit product format
- 578260420
- Labeler code
- 57826
- Product ID
- 57826-420_ba5d3100-49aa-2fd0-e053-2a95a90aec1b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- TRISODIUM CITRATE DIHYDRATE
- Dosage form
- SOLUTION
- Route
- EXTRACORPOREAL
- Labeler
- Haemonetics Corporation
- Application
- BN980123
- Marketing category
- NDA
- Marketing start
- 2013-01-10
- Marketing end
- 0000-00-00
- Substance
- TRISODIUM CITRATE DIHYDRATE
- Active strength
- 40 mg/mL
- Pharmacologic classes
- Acidifying Activity [MoA],Calculi Dissolution Agent [EPC],Anti-coagulant [EPC],Decreased Coagulation Factor Activity [PE],Calcium Chelating Activity [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 57826-420-02 | 57826042002 | 250 mL in 1 BAG (57826-420-02) | 250 ml | 2013-01-10 | 0000-00-00 | No | No | Current |