FDA.reportPublic FDA data

NDC 50090-2159-01 - Cefuroxime axetil

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
50090-2159
Requested NDC
50090-2159-01
Package NDCs from labels
50090-2159-0, 50090-2159-1, 50090-2159-01
Manufacturer
A-S Medication Solutions
Effective date
2024-09-11
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Cefuroxime axetil - A-S Medication SolutionsA-S Medication Solutions2024-09-11Human Prescription Drug Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50090-2159-02023-02-07C16284748780-1f386c649-b15d-0266-e053-dadaa90a7c1aThese highlights do not include all the information needed to use CEFUROXIME AXETIL TABLETS safely and effectively. See full prescribing information for CEFUROXIME AXETIL TABLETS. CEFUROXIME AXETIL tablets, for oral use Initial U.S. Approval: 1987
50090-2159-02023-01-30C16284748780-1f386c649-b15d-0266-e053-dadaa90a7c1aThese highlights do not include all the information needed to use CEFUROXIME AXETIL TABLETS safely and effectively. See full prescribing information for CEFUROXIME AXETIL TABLETS. CEFUROXIME AXETIL tablets, for oral use Initial U.S. Approval: 1987

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50090-2159-0Cefuroxime axetil20 in 1 BOTTLETABLET, FILM COATED2017
50090-2159-1Cefuroxime axetil14 in 1 BOTTLETABLET, FILM COATED1417

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50090-2159CEFUROXIME AXETIL TABLET, FILM COATED [A-S MEDICATION SOLUTIONS]17Current NDC, Legacy NDC, 2 package rows20240912_84593261-838c-433a-8d9d-1d37b11058da.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-2159-0EA - Each50090-2159f4d63fcb-70fb-436f-a5a9-c617e939008f12019-02-13
50090-2159-1EA - Each50090-2159e40d5dc7-98e2-4654-831e-294d6ad2171a12024-10-04

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 72 of 172 · 3,433 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Cherry Antacid Soft ChewsCALCIUM CARBONATECVS Pharmacy61e4e83c-ee98-579d-e053-2991aa0ab0992025-12-07WarningsExact identifier
unii: H0G9379FGK
CVS Mixed Berry Antacid HBG 54ctCALCIUM CARBONATECVS Pharmacye9204edb-e4d9-3975-e053-2995a90ac6a92025-12-07WarningsExact identifier
unii: H0G9379FGK
CVS Mixed Berry Antacid HBG 28ctCALCIUM CARBONATECVS Pharmacye9481d36-3b28-5caf-e053-2a95a90a31212025-12-07WarningsExact identifier
unii: H0G9379FGK
CVS Wild Berry Antacid ChewsCALCIUM CARBONATECVS Pharmacyf6f45d9c-f9fc-225b-e053-6394a90a30e12025-12-07WarningsExact identifier
unii: H0G9379FGK
CVS Wild Berry Antacid ChewsCALCIUM CARBONATECVS Pharmacyf6f5dc9a-b573-70c1-e053-6394a90acdb02025-12-07WarningsExact identifier
unii: H0G9379FGK
Basic Care Antacid Fruit ChewsCALCIUM CARBONATEAmazon.comc8d2b8aa-fce4-f973-e053-2995a90a6edd2025-12-05WarningsExact identifier
unii: H0G9379FGK
Basic Care Berry Antacid HBGCALCIUM CARBONATEAmazon.comc8d4050e-75fd-2445-e053-2995a90a7b0d2025-12-05WarningsExact identifier
unii: H0G9379FGK
CVS Health Maximum StrengthANTACID AND ANTIGASCVS Pharmacy,Inc.0a13ac81-0c63-48c1-bbb0-f6e67f97b8962025-12-04WarningsExact identifier
unii: H0G9379FGK
QUALITY CHOICE Regular StrengthANTACID TABLETS (CALCIUM CARBONATE)QUALITY CHOICE (Chain drug Marketing Assoiciation)fce6c50d-908f-44a6-ba63-ece813f3711b2025-12-04WarningsExact identifier
unii: H0G9379FGK
QUALITY CHOICE Regular StrengthANTACID TABLETS (CALCIUM CARBONATE)QUALITY CHOICE (Chain drug Marketing Assoiciation)667ffb59-9bff-45a7-89f0-ccfa0d8419092025-12-04WarningsExact identifier
unii: H0G9379FGK
QUALITY CHOICECALCIUM CARBONATEQUALITY CHOICE (Chain drug Marketing Assoiciation)9ff282fd-7623-4c9e-8faa-c51e33a7616e2025-12-04WarningsExact identifier
unii: H0G9379FGK
QUALITY CHOICE Extra StrengthANTACID TABLETS (CALCIUM CARBONATE)QUALITY CHOICE (Chain drug Marketing Assoiciation)7c948dc6-e569-46d2-8edd-59da48857e0e2025-12-04WarningsExact identifier
unii: H0G9379FGK
QUALITY CHOICE Ultra StrengthANTACID TABLETS (CALCIUM CARBONATE)QUALITY CHOICE (Chain drug Marketing Assoiciation)b074a885-5d10-46e4-8de9-dd9460968dad2025-12-04WarningsExact identifier
unii: H0G9379FGK
Quality Choice Extra StrengthANTACID TABLETS (CALCIUM CARBONATE)QUALITY CHOICE (Chain drug Marketing Assoiciation)2bb8ccb6-6275-4ace-8096-ee545501df392025-12-04WarningsExact identifier
unii: H0G9379FGK
Quality Choice Ultra StrengthANTACID TABLET (CALCIUM CARBONATE)QUALITY CHOICE (Chain drug Marketing Assoiciation)cdac56f1-e579-4943-a24a-6564c30086d22025-12-04WarningsExact identifier
unii: H0G9379FGK
Solbar Shield SPF40SOLBAR SHIELD SPF40Person and Coveybd3a9a94-fc87-4127-abf9-29e56ac9ce5d2025-12-04WarningsExact identifier
unii: 15FIX9V2JP
Alka-Seltzer Heartburn Relief PeppermintCALCIUM CARBONATEBayer HealthCare LLC.9b8e802f-91b6-4559-e053-2a95a90aff672025-12-04WarningsExact identifier
unii: H0G9379FGK
Alka-Seltzer Cool Action Heartburn Relief MintCALCIUM CARBONATEBayer HealthCare LLC.9b8da147-8d0c-e6b0-e053-2a95a90a35e62025-12-04WarningsExact identifier
unii: H0G9379FGK
Alka-Seltzer Kids Tummy ReliefChewsCALCIUM CARBONATE AND DIMETHICONEBayer HealthCare LLC.ba48966e-3762-5fdf-e053-2995a90aeb3d2025-12-04WarningsExact identifier
unii: H0G9379FGK
Alka-Seltzer Extra Strength Heartburn ReliefChewsCALCIUM CARBONATEBayer HealthCare LLC.51759451-63a8-0fb4-e054-00144ff8d46c2025-12-04WarningsExact identifier
unii: H0G9379FGK

Reported adverse events (FAERS/openFDA)#

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