Sodium Citrate Blood-Pack Units, (PL 146 Plastic)
- Product NDC
- 0942-9502
- 11-digit product format
- 009429502
- Labeler code
- 0942
- Product ID
- 0942-9502_a79448cc-6eb2-413e-bb5d-4d51ef911f58
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Anticoagulant Sodium Citrate Solution
- Dosage form
- SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Fenwal, Inc.
- Application
- BN770923
- Marketing category
- NDA
- Marketing start
- 2007-03-01
- Marketing end
- 2022-01-31
- Substance
- TRISODIUM CITRATE DIHYDRATE
- Active strength
- 2 g/50mL
- 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
- 0000-00-00
- 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 |
|---|
| 0942-9502-06 | 00942950206 | 50 mL in 1 BAG (0942-9502-06) | 50 ml | 2007-03-01 | 2022-01-31 | No | No | Current |