FDA.reportPublic FDA data

NDC 51072-108-00 - Altren

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
51072-108
Requested NDC
51072-108-00
Package NDCs from labels
51072-108-00
Manufacturer
Aurora Pharmaceutical, Inc.
Effective date
2024-10-09
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Altren ® Solution 0.22% (altrenogest)Aurora Pharmaceutical, Inc.2024-10-09PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51072-108-00Altren1000 mL in 1 BOTTLESOLUTION10003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51072-108ALTREN (ALTRENOGEST) SOLUTION [AURORA PHARMACEUTICAL, INC.]31 package rows20241011_e3c9b97e-a025-47e8-83e7-b7e66522c800.zip

Reported adverse events (FAERS/openFDA)#

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