NDC product
Anticoagulant Citrate Phosphate Dextrose (CPD) Blood-Pack Units in PL 146 Plastic
NDC 0942-9202 · Fenwal, Inc.
Key facts
| Product NDC | 0942-9202 |
|---|---|
| Proprietary name | Anticoagulant Citrate Phosphate Dextrose (CPD) Blood-Pack Units in PL 146 Plastic |
| Nonproprietary name | Anticoagulant Citrate Phosphate Dextrose (CPD) |
| Substances | TRISODIUM CITRATE DIHYDRATE, DEXTROSE MONOHYDRATE, ANHYDROUS CITRIC ACID, SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE |
| Dosage form | SOLUTION |
| Route | INTRAVENOUS |
| Labeler | Fenwal, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Application number | BN170401 |
| Pharmacologic classes | Acidifying Activity [MoA], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE] |
| Marketing start | Mar 31, 2007 |
| Listing certified through | Dec 31, 2026 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: