NDC 51072-140 - OvuGel
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
- 51072-140
- Package NDCs from labels
- 51072-140-00
- Manufacturer
- Aurora Pharmaceutical, Inc.
- Effective date
- 2026-03-09
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| OvuGel | Aurora Pharmaceutical, Inc. | 2026-03-09 | OTC ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51072-140-00 | OvuGel | 52.5 mL in 1 BOTTLE | GEL | 52.5 | 2 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.