NDC 51233-101-50 - 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
- 51233-101
- Requested NDC
- 51233-101-50
- Package NDCs from labels
- 51233-101-50
- Manufacturer
- United-AH II, LLC
- Effective date
- 2026-04-29
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| OvuGel - United-AH II, LLC | United-AH II, LLC | 2026-04-29 | OTC ANIMAL DRUG LABEL |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| Triptorelin Acetate | ACTIVE INGREDIENT | 43OFW291R9 | OVUGEL (TRIPTORELIN ACETATE) GEL [JBS UNITED ANIMAL HEALTH II LLC (FORMERLY, PENNATEK LLC)] | 3 | |
| Triptorelin | ACTIVE MOIETY | 9081Y98W2V | OVUGEL (TRIPTORELIN ACETATE) GEL [JBS UNITED ANIMAL HEALTH II LLC (FORMERLY, PENNATEK LLC)] | 3 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.