FDA.reportPublic FDA data

Romifidine Hydrochloride

Manufacturer
AX Pharmaceutical Corp
Effective date
2019-06-05
Label type
BULK INGREDIENT
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:22:47

Label at a glance#

ProductRomifidine Hydrochloride
Active ingredientROMIFIDINE HYDROCHLORIDE
Label structure1 sections

Label contents#

Full prescribing information#

Romifidine Hydrochloride

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62157-85462157-854-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
NameUNIIKind
ROMIFIDINE HYDROCHLORIDE98LQ6RS0TAACTIM

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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