FDA.reportPublic FDA data

NDC 80425-0072-01 - Ondansetron HCL

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
80425-0072
Requested NDC
80425-0072-01
Package NDCs from labels
80425-0072-5, 80425-0072-1, 80425-0072-2, 80425-0072-3, 80425-0072-4, 80425-0072-01
Manufacturer
Advanced Rx of Tennessee, LLC
Effective date
2024-12-31
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Ondansetron HCL - Advanced Rx of Tennessee, LLCAdvanced Rx of Tennessee, LLC2024-12-31HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80425-0072-1Ondansetron HCL20 in 1 BOTTLETABLET, FILM COATED209
80425-0072-2Ondansetron HCL30 in 1 BOTTLETABLET, FILM COATED309
80425-0072-3Ondansetron HCL60 in 1 BOTTLETABLET, FILM COATED609
80425-0072-4Ondansetron HCL15 in 1 BOTTLETABLET, FILM COATED159
80425-0072-5Ondansetron HCL10 in 1 BOTTLETABLET, FILM COATED109

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80425-0072ONDANSETRON HCL TABLET, FILM COATED [ADVANCED RX OF TENNESSEE, LLC]9Current NDC, Legacy NDC, 5 package rows20250101_af830edc-ce9e-b038-e053-2a95a90ae974.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
80425-0072-1EA - Each80425-0072f4f9f643-eb37-4145-83cb-feb17bc5b76a12023-04-07
80425-0072-2EA - Each80425-0072963d3daf-a33f-463a-a86a-ac0f4878cdf912023-04-07
80425-0072-3EA - Each80425-0072f09d67c1-00d4-47c5-8212-9f8984d0d4a712023-04-07
80425-0072-4EA - Each80425-007203a60e58-449c-4086-bf8a-5aafe67c9dca12023-04-07
80425-0072-5EA - Each80425-0072778a40a8-6800-43d1-b8c7-9e52e8b8a7fb12023-04-07

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 8 of 8 · 141 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Ondansetron HydrochlorideONDANSETRON HYDROCHLORIDEAphena Pharma Solutions - Tennessee, LLC08db5ce7-4dcf-4581-a0bf-f405cc22b48d2018-08-27Warnings, Adverse reactionsExact identifier
application number: ANDA078539
rxcui: 312086
unii: NMH84OZK2B

Reported adverse events (FAERS/openFDA)#

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