NDC product
Sodium Chloride
NDC 79672-613 · Nextgen Pharmaceuticals LLC
Key facts
| Product NDC | 79672-613 |
|---|---|
| Proprietary name | Sodium Chloride |
| Nonproprietary name | SODIUM CHLORIDE |
| Substances | SODIUM CHLORIDE |
| Dosage form | INJECTION, SOLUTION |
| Route | INTRAVENOUS |
| Labeler | Nextgen Pharmaceuticals LLC |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA207956 |
| Marketing start | May 25, 2017 |
| 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: