NDC 73377-074 - Sirolimus

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
73377-074
Package NDCs from labels
73377-074-01, 73377-074-02, 73377-074-03
Manufacturer
AX Pharmaceutical Corp
Effective date
2026-06-26
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Sirolimus - AX Pharmaceutical CorpAX Pharmaceutical Corp2026-06-26BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73377-074-01Sirolimus10 g in 1 JARPOWDER103
73377-074-02Sirolimus100 g in 1 JARPOWDER1003
73377-074-03Sirolimus5 g in 1 JARPOWDER53

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73377-074SIROLIMUS POWDER [AX PHARMACEUTICAL CORP]33 package rows20250214_1b1bd16b-5989-4d8a-a63d-ea911383852e.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 2 of 2 · 22 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
sirolimusSIROLIMUSZydus Pharmaceuticals USA Inc.ec473170-47f1-4a5c-b4d9-ac36406ed2412023-07-20Boxed warning, Warnings, Adverse reactionsExact identifier
unii: W36ZG6FT64
SirolimusSIROLIMUSAmneal Pharmaceuticals NY LLCa522b5e1-fe51-4eb8-9657-3b1d6af8dfd52022-12-22Boxed warning, Warnings, Adverse reactionsExact identifier
unii: W36ZG6FT64

Reported adverse events (FAERS/openFDA)#

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