NDC 51072-087-00 - 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: 51072-087
Requested NDC: 51072-087-00
Package NDCs from labels: 51072-087-00
Manufacturer: Aurora Pharmaceutical, Inc.
Effective date: 2026-03-26
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
OvuGel®	Aurora Pharmaceutical, Inc.	2026-03-26	OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
51072-087-00	OvuGel	52.5 mL in 1 BOTTLE	GEL	52.5		2
51072-087-00	OvuGel	1 in 1 CARTON	GEL	1		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51072-087	OVUGEL (TRIPTORELIN ACETATE) GEL [AURORA PHARMACEUTICAL, INC.]	1	Unmatched	20230616_bcb5b01b-b5bb-46a9-b844-2a9799013325.zip

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.