FDA.reportPublic FDA data

NDC 73377-022-02 - Altrenogest

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
73377-022
Requested NDC
73377-022-02
Package NDCs from labels
73377-022-01, 73377-022-02
Manufacturer
AX Pharmaceutical Corp
Effective date
2026-03-10
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Altrenogest - AX Pharmaceutical CorpAX Pharmaceutical Corp2026-03-10BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73377-022-01Altrenogest250 g in 1 JARPOWDER2505
73377-022-02Altrenogest240 g in 1 JARPOWDER2405

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73377-022ALTRENOGEST POWDER [AX PHARMACEUTICAL CORP]42 package rows20231003_478592f1-968e-4698-9af8-24a1a3cceaae.zip

Reported adverse events (FAERS/openFDA)#

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