FDA.reportPublic FDA data

NDC 62157-854-01 - Romifidine Hydrochloride

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
62157-854
Requested NDC
62157-854-01
Package NDCs from labels
62157-854-02, 62157-854-01
Manufacturer
AX Pharmaceutical Corp
Effective date
2019-06-05
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Romifidine Hydrochloride - AX Pharmaceutical CorpAX Pharmaceutical Corp2019-06-05BULK INGREDIENT
Romifidine Hydrochloride - AX Pharmaceutical CorpAX Pharmaceutical Corp2019-06-04BULK INGREDIENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62157-854-01Romifidine Hydrochloride100 g in 1 JARPOWDER1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62157-854ROMIFIDINE HYDROCHLORIDE POWDER [AX PHARMACEUTICAL CORP]11 package rows20190605_5ca39520-54b7-4e38-942e-6e15397dcd86.zip

Reported adverse events (FAERS/openFDA)#

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