NDC 50989-745-86 - Novox
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 50989-745
- Requested NDC
- 50989-745-86
- Package NDCs from labels
- 50989-745-86, 50989-745-50
- Manufacturer
- VEDCO INC
- Effective date
- 2026-03-23
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Novox - VEDCO INC | VEDCO INC | 2026-03-23 | PRESCRIPTION ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50989-745-50 | Novox | 60 in 1 BOTTLE, PLASTIC | TABLET | 60 | 4 | |
| 50989-745-86 | Novox | 180 in 1 BOTTLE, PLASTIC | TABLET | 180 | 4 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Vedlube | MINERAL OIL AND WHITE PETROLATUM LUBRICANT EYE OINTMENT | VEDCO INC | 55d126fa-7489-4307-824e-b6957e57d4e9 | 2026-07-31 | Warnings | VEDCO INC |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.