FDA.reportPublic FDA data

Zithromax TRI-PAK, 3 Count

RxCUI
750157
RxNorm name
Zithromax TRI-PAK, 3 Count
Display name
Zithromax TRI-PAK, 3 Count
Full name
Zithromax TRI-PAK, 3 Count
Term type
PSN
Status
DailyMed mapping
Updated
2026-06-04 23:39:23

RxNav Current And Historical NDCs#

RxNav current and historical NDC rows page 1 of 1 · 0 matching rows.

No records found.

UNII Substances#

UNII substance links page 1 of 1 · 0 matching rows.

No records found.

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 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ZithromaxAZITHROMYCIN DIHYDRATEPfizer Laboratories Div Pfizer Incdb52b91e-79f7-4cc1-9564-f2eee8e31c452026-07-24Warnings, Adverse reactionsExact identifier
rxcui: 750157

DailyMed RxNorm Mappings#

unique DailyMed labels mapped to this RxNorm concept page 1 of 1 · 1 matching rows.

Set ID, RxNorm mappings, Terms table
Set IDRxNorm mappingsTermsSPL versionLabelEffective
db52b91e-79f7-4cc1-9564-f2eee8e31c45{3 (azithromycin 500 MG Oral Tablet [Zithromax]) } Pack [TRI-PAK] [BPCK] · Zithromax TRI-PAK, 3 Count [PSN] · TRI-PAK [SY]348These highlights do not include all the information needed to use ZITHROMAX ® safely and effectively. See full prescribing information for ZITHROMAX. ZITHROMAX (azithromycin) 250 mg and 500 mg tablets, for oral use ZITHROMAX (azithromycin) for oral suspension Initial U.S. Approval: 199120260107