NDC 16590-215 - 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
16590-215
Package NDCs from labels
16590-215-20
Manufacturer
STAT Rx USA LLC | PSS World Medical Inc.
Effective date
2012-08-30
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
PRODUCT INFORMATION Cefuroxime Axetil Tablets, USPSTAT Rx USA LLC | PSS World Medical Inc.2012-08-30HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
16590-215-202019-11-13C16284748780-197449f38-bc24-f6ea-e053-dbdaa90aa703PRODUCT INFORMATION Cefuroxime Axetil Tablets, USP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
16590-215-20CEFUROXIME AXETIL20 in 1 BOTTLETABLET, FILM COATED201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
16590-215CEFUROXIME AXETIL TABLET, FILM COATED [STAT RX USA LLC]11 package rows20120831_8dce5b09-9b27-457b-994e-0f7cad674a3c.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
16590-215-20EA - Each16590-215bac1cad7-bef9-47b3-8b5e-24178a0ba6b612013-02-13

DailyMed Socrata Ingredients#