NDC product
Leucoflex CGP
NDC 14498-002 · Maco Productions
Key facts
| Product NDC | 14498-002 |
|---|---|
| Proprietary name | Leucoflex CGP |
| Nonproprietary name | Anticoagulant Citrate Phosphate Dextrose Solution with Additive Solution AS-1 |
| Dosage form | KIT |
| Labeler | Maco Productions |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Application number | BN040083 |
| Marketing start | May 31, 2013 |
| 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: