NDC 73309-025-01 - Cefpodoxime Proxetil

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
73309-025
Requested NDC
73309-025-01
Package NDCs from labels
73309-025-01, 73309-025-02, 73309-025-03
Manufacturer
BLUEBAY SHANDONG CO.,LTD
Effective date
2021-10-28
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Cefpodoxime Proxetil - BLUEBAY SHANDONG CO.,LTDBLUEBAY SHANDONG CO.,LTD2021-10-28BULK INGREDIENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73309-025-01Cefpodoxime Proxetil500 g in 1 PACKAGEPOWDER5003
73309-025-02Cefpodoxime Proxetil250 g in 1 JARPOWDER2503
73309-025-03Cefpodoxime Proxetil50 g in 1 JARPOWDER503

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73309-025CEFPODOXIME PROXETIL POWDER [BLUEBAY SHANDONG CO.,LTD]33 package rows20211030_a30f855a-3e06-458e-99dd-7c16f8110fbd.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 1 of 1 ยท 15 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
CEFPODOXIME PROXETILCEFPODOXIME PROXETILRedpharm Drug59d848e9-de7a-669b-e063-6394a90a2b352026-08-25Warnings, Adverse reactionsExact identifier
unii: 2TB00A1Z7N
Cefpodoxime ProxetilCEFPODOXIME PROXETILSandoz Inc8519a9d8-7106-4545-bc58-859ee9a6708e2026-07-30Warnings, Adverse reactionsExact identifier
unii: 2TB00A1Z7N
Cefpodoxime ProxetilCEFPODOXIME PROXETILREMEDYREPACK INC.dae9cbf2-65b5-49fa-898b-924c39b86c572026-06-04Warnings, Adverse reactionsExact identifier
unii: 2TB00A1Z7N
Cefpodoxime ProxetilCEFPODOXIME PROXETILRising Pharma Holdings, Inc.edf589b2-f796-4522-a5e6-2bd0a833922f2025-06-06Warnings, Adverse reactionsExact identifier
unii: 2TB00A1Z7N
Cefpodoxime ProxetilCEFPODOXIME PROXETILGolden State Medical Supply, Inc.fb313728-09f1-aff8-e053-6394a90a30a82025-02-18Warnings, Adverse reactionsExact identifier
unii: 2TB00A1Z7N
Cefpodoxime ProxetilCEFPODOXIME PROXETILNuCare Pharmaceuticals,Inc.fe827f61-9336-72e7-e053-6394a90af75f2025-02-06Warnings, Adverse reactionsExact identifier
unii: 2TB00A1Z7N
Cefpodoxime ProxetilCEFPODOXIME PROXETILNuCare Pharmaceuticals,Inc.1b405104-650b-c8e3-e063-6294a90a9e8a2024-06-19Warnings, Adverse reactionsExact identifier
unii: 2TB00A1Z7N
CEFPODOXIME PROXETILCEFPODOXIME PROXETILCronus Pharma LLCbc9c338c-1fc7-4bc2-a357-a78e433cbe9d2024-01-04Warnings, Adverse reactionsExact identifier
unii: 2TB00A1Z7N
Cefpodoxime ProxetilCEFPODOXIME PROXETILNorthStar Rx LLC5310de78-22c3-4bee-9956-854e767b6bef2024-01-04Warnings, Adverse reactionsExact identifier
unii: 2TB00A1Z7N
Cefpodoxime ProxetilCEFPODOXIME PROXETILAurobindo Pharma Limited63777889-d306-4fc3-88da-b24859040ef42024-01-04Warnings, Adverse reactionsExact identifier
unii: 2TB00A1Z7N
CEFPODOXIME PROXETILCEFPODOXIME PROXETILAurobindo Pharma Limitedc36f2137-98bb-4583-89f7-6bce9582c4652024-01-03Warnings, Adverse reactionsExact identifier
unii: 2TB00A1Z7N
CEFPODOXIME PROXETILCEFPODOXIME PROXETILNorthStar Rx LLC4587a7c1-cd6c-4946-a0dd-fcfe0c8504b92024-01-03Warnings, Adverse reactionsExact identifier
unii: 2TB00A1Z7N
Cefpodoxime ProxetilCEFPODOXIME PROXETILAmici Pharmaceuticals, LLC.9d6d7f50-9838-47e3-8214-53e2dbeeadea2023-07-13Warnings, Adverse reactionsExact identifier
unii: 2TB00A1Z7N
Cefpodoxime ProxetilCEFPODOXIME PROXETILAscend Laboratories, LLCce5646cb-a450-4c2c-8499-6ecf71b12b0e2023-04-14Warnings, Adverse reactionsExact identifier
unii: 2TB00A1Z7N
Cefpodoxime ProxetilCEFPODOXIME PROXETILAscend Laboratories, LLC5d5ca5b6-282b-4683-908c-8547822557392022-05-20Warnings, Adverse reactionsExact identifier
unii: 2TB00A1Z7N

Reported adverse events (FAERS/openFDA)#

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