NDC product
Retaine Ultra PF
NDC 54799-470 · OCuSOFT LLC
Key facts
| Product NDC | 54799-470 |
|---|---|
| Proprietary name | Retaine Ultra PF |
| Nonproprietary name | Polyethylene Glycol |
| Substances | POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL |
| Dosage form | LIQUID |
| Route | OPHTHALMIC |
| Labeler | OCuSOFT LLC |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M018 |
| Marketing start | May 19, 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: