NDC product
DEXTROSE MONOHYDRATE
NDC 51662-1453 · HF Acquisition Co LLC, DBA HealthFirst
Key facts
| Product NDC | 51662-1453 |
|---|---|
| Proprietary name | DEXTROSE MONOHYDRATE |
| Labeler | HF Acquisition Co LLC, DBA HealthFirst |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing start | Jan 11, 2020 |
| Marketing end | Aug 21, 2026 |
| Listing certified through | Aug 21, 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: