NDC product
Nacl 0.9% Normal Saline Solution
NDC 87974-101 · CHI FUNG TECHNOLOGY COMPANY
Key facts
| Product NDC | 87974-101 |
|---|---|
| Proprietary name | Nacl 0.9% Normal Saline Solution |
| Nonproprietary name | Sodium Chloride |
| Substances | SODIUM CHLORIDE |
| Dosage form | SOLUTION |
| Route | NASAL, TOPICAL |
| Labeler | CHI FUNG TECHNOLOGY COMPANY |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Pharmacologic classes | Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC] |
| Marketing start | Aug 31, 2026 |
| 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: