NDC product
MTL1 Leucoflex
NDC 14498-001 · Maco Productions
Key facts
| Product NDC | 14498-001 |
|---|---|
| Proprietary name | MTL1 Leucoflex |
| Nonproprietary name | Anticoagulant Citrate Phosphate Dextrose Solution with AS-1 |
| Dosage form | KIT |
| Route | INTRAVENOUS |
| Labeler | Maco Productions |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Application number | BN040083 |
| Marketing start | Nov 21, 2005 |
| 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: