{18 (oteseconazole 150 MG Oral Capsule) } Pack

RxCUI
2605802
RxNorm name
{18 (oteseconazole 150 MG Oral Capsule) } Pack
Display name
{18 (oteseconazole 150 MG Oral Capsule) } Pack
Full name
{18 (oteseconazole 150 MG Oral Capsule) } Pack
Term type
GPCK
Status
DailyMed mapping
Updated
2026-06-04 23:39:25

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
VIVJOAOTESECONAZOLEMycovia Pharmaceuticals, Inc.e21d5008-800e-4417-927f-14340341865f2026-01-08Warnings, Adverse reactionsExact identifier
rxcui: 2605802

DailyMed RxNorm Mappings#

Set ID, RxNorm string, TTY table
Set IDRxNorm stringTTYSPL versionLabelEffective
e21d5008-800e-4417-927f-14340341865f{18 (oteseconazole 150 MG Oral Capsule) } PackGPCK5These highlights do not include all the information needed to use VIVJOA™ safely and effectively. See full prescribing information for VIVJOA™. VIVJOA™ (oteseconazole) capsules, for oral use Initial U.S. Approval: 202220260108
e21d5008-800e-4417-927f-14340341865foteseconazole 150 MG 18-Count PackPSN5These highlights do not include all the information needed to use VIVJOA™ safely and effectively. See full prescribing information for VIVJOA™. VIVJOA™ (oteseconazole) capsules, for oral use Initial U.S. Approval: 202220260108
e21d5008-800e-4417-927f-14340341865foteseconazole 150 MG 18-Count PackSY5These highlights do not include all the information needed to use VIVJOA™ safely and effectively. See full prescribing information for VIVJOA™. VIVJOA™ (oteseconazole) capsules, for oral use Initial U.S. Approval: 202220260108