NDC product
Childrens Loratadine Oral
NDC 17856-6767 · Atlantic Biologicals
Key facts
| Product NDC | 17856-6767 |
|---|---|
| Proprietary name | Childrens Loratadine Oral |
| Nonproprietary name | Loratadine |
| Substances | LORATADINE |
| Dosage form | SOLUTION |
| Route | ORAL |
| Labeler | Atlantic Biologicals |
| Product type | HUMAN OTC DRUG |
| Marketing category | ANDA |
| Application number | ANDA075728 |
| Marketing start | Feb 12, 2019 |
| Listing certified through | Dec 31, 2027 |
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: