FDA.reportPublic FDA data

Doryx 60 MG Delayed Release Oral Tablet

RxCUI
1801144
RxNorm name
Doryx 60 MG Delayed Release Oral Tablet
Display name
Doryx 60 MG Delayed Release Oral Tablet
Full name
Doryx 60 MG Delayed Release Oral Tablet
Term type
PSN
Status
DailyMed mapping
Updated
2026-06-04 23:39:29

RxNav Current And Historical NDCs#

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No records found.

UNII Substances#

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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
DORYX MPCDOXYCYCLINE HYCLATEMayne Pharma Commercial LLCf9277bb8-982d-444d-9325-35d5c53a2d352026-02-16Warnings, Adverse reactionsExact identifier
rxcui: 1801144

DailyMed RxNorm Mappings#

Set ID, RxNorm string, TTY table
Set IDRxNorm stringTTYSPL versionLabelEffective
f9277bb8-982d-444d-9325-35d5c53a2d35Doryx 60 MG Delayed Release Oral TabletPSN15These highlights do not include all the information needed to use DORYX MPC safely and effectively. See full prescribing information for DORYX MPC DORYX MPC (doxycycline hyclate delayed-release tablets), for oral use. Initial U.S. Approval: 196720260216
f9277bb8-982d-444d-9325-35d5c53a2d35Doryx 60 MG Delayed Release Oral TabletSY15These highlights do not include all the information needed to use DORYX MPC safely and effectively. See full prescribing information for DORYX MPC DORYX MPC (doxycycline hyclate delayed-release tablets), for oral use. Initial U.S. Approval: 196720260216
f9277bb8-982d-444d-9325-35d5c53a2d35doxycycline hyclate 60 MG Delayed Release Oral Tablet [Doryx]SBD15These highlights do not include all the information needed to use DORYX MPC safely and effectively. See full prescribing information for DORYX MPC DORYX MPC (doxycycline hyclate delayed-release tablets), for oral use. Initial U.S. Approval: 196720260216