FDA.reportPublic FDA data

Lo-Zumandimine 28 Day Pack

RxCUI
2003375
RxNorm name
Lo-Zumandimine 28 Day Pack
Display name
Lo-Zumandimine 28 Day Pack
Full name
Lo-Zumandimine 28 Day Pack
Term type
PSN
Status
DailyMed mapping
Updated
2026-06-04 23:39:14

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
Lo-ZumandimineDROSPIRENONE AND ETHINYL ESTRADIOLAurobindo Pharma Limiteda8c718cc-e235-4710-a9e6-6c58433f30282023-10-09Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 2003375

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
a8c718cc-e235-4710-a9e6-6c58433f3028{24 (drospirenone 3 MG / ethinyl estradiol 0.02 MG Oral Tablet) / 4 (inert ingredients 1 MG Oral Tablet) } Pack [Lo-Zumandimine 28 Day] [BPCK] · Lo-Zumandimine 28 Day Pack [PSN] · Lo-Zumandimine 28 Day Pack [SY]39These highlights do not include all the information needed to use LO-ZUMANDIMINE safely and effectively. See full prescribing information for LO-ZUMANDIMINE. LO-ZUMANDIMINE™ (drospirenone and ethinyl estradiol) tablets, for oral use Initial U.S. Approval: 200120231009