FDA.reportPublic FDA data

NDC 73309-300 - Doxapram Hydrochloride Monohydrate

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
73309-300
Package NDCs from labels
73309-300-01
Manufacturer
BLUEBAY SHANDONG CO.,LTD
Effective date
2021-06-01
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Doxapram Hydrochloride Monohydrate - BLUEBAY SHANDONG CO.,LTDBLUEBAY SHANDONG CO.,LTD2021-06-01BULK INGREDIENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73309-300-01Doxapram Hydrochloride Monohydrate50 g in 1 JARPOWDER501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73309-300DOXAPRAM HYDROCHLORIDE MONOHYDRATE POWDER [BLUEBAY SHANDONG CO.,LTD]11 package rows20210602_9c0af8e1-ced3-41d1-a7d7-771b7520bb92.zip

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 ยท 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
DOXAPRAM HYDROCHLORIDEDOXAPRAM HYDROCHLORIDEHF Acquisition Co LLC, DBA HealthFirst954859c0-a121-34d6-e053-2a95a90a1e192025-01-08Warnings, Adverse reactionsExact identifier
unii: P5RU6UOQ5Y
DopramDOXAPRAM HYDROCHLORIDEHikma Pharmaceuticals USA Inc.b8eb330a-a75b-46cb-b694-5be9327ed2eb2024-04-09Warnings, Adverse reactionsExact identifier
unii: P5RU6UOQ5Y

Reported adverse events (FAERS/openFDA)#

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