FDA.reportPublic FDA data

NDC 73377-003-01 - Mirtazapine Hemihydrate

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
73377-003
Requested NDC
73377-003-01
Package NDCs from labels
73377-003-01
Manufacturer
AX Pharmaceutical Corp
Effective date
2026-01-16
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Mirtazapine Hemihydrate - AX Pharmaceutical CorpAX Pharmaceutical Corp2026-01-16BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73377-003-01Mirtazapine Hemihydrate1 kg in 1 JARPOWDER13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73377-003MIRTAZAPINE HEMIHYDRATE POWDER [AX PHARMACEUTICAL CORP]21 package rows20211112_a6d26cd1-3a3e-443e-9f87-5d8c1ce00b61.zip

Reported adverse events (FAERS/openFDA)#

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