FDA.reportPublic FDA data

romifidine hcl

Manufacturer
BLUEBAY SHANDONG CO.,LTD
Effective date
2020-12-02
Label type
BULK INGREDIENT
Version
3
Source
full-release
Hydrated at
2026-06-01 02:49:47

Label at a glance#

Productromifidine hcl
Active ingredientROMIFIDINE HYDROCHLORIDE
Label structure1 sections

Label contents#

Full prescribing information#

romifidine hcl

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73309-152-01romifidine hcl10 g in 1 JARPOWDER103
73309-152-02romifidine hcl5 g in 1 JARPOWDER53
73309-152-03romifidine hcl100 g in 1 JARPOWDER1003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73309-152ROMIFIDINE HCL POWDER [BLUEBAY SHANDONG CO.,LTD]33 package rows20201203_502ad59c-ff0d-42f0-97de-d22a9b907eea.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73309-15273309-152-01, 73309-152-02, 73309-152-03

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 HYDROCHLORIDE98LQ6RS0TAACTIB

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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