FDA.reportPublic FDA data

NDC 51072-086-00 - SwineMate

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
51072-086
Requested NDC
51072-086-00
Package NDCs from labels
51072-086-00
Manufacturer
Aurora Pharmaceutical, Inc.
Effective date
2024-06-21
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
SwineMate ® (altrenogest)Aurora Pharmaceutical, Inc.2024-06-21OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51072-086-00SwineMate1000 mL in 1 BOTTLESOLUTION100010

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51072-086SWINEMATE (ALTRENOGEST) SOLUTION [AURORA PHARMACEUTICAL, INC.]101 package rows20240704_1a3188f0-8eb8-42db-b8fb-1b1eb659065d.zip

Reported adverse events (FAERS/openFDA)#

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