NDC 73309-092-01 - Primaquine Phosphate

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
73309-092
Requested NDC
73309-092-01
Package NDCs from labels
73309-092-01
Manufacturer
BLUEBAY SHANDONG CO.,LTD
Effective date
2020-02-28
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Primaquine Phosphate - BLUEBAY SHANDONG CO.,LTDBLUEBAY SHANDONG CO.,LTD2020-02-28BULK INGREDIENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73309-092-01Primaquine Phosphate100 g in 1 JARPOWDER1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73309-092PRIMAQUINE PHOSPHATE POWDER [BLUEBAY SHANDONG CO.,LTD]11 package rows20200229_a6d218f6-3f8a-47d9-a116-e109ac0dfdc4.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 4 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Primaquine PhosphatePRIMAQUINE PHOSPHATEPD-Rx Pharmaceuticals, Inc.3f16166d-678e-51aa-e054-00144ff88e882026-05-12Warnings, Adverse reactionsExact identifier
unii: H0982HF78B
PRIMAQUINE PHOSPHATEPRIMAQUINE PHOSPHATEAvKARE82465385-4602-7f46-e053-2991aa0a9fdf2026-02-25Warnings, Adverse reactionsExact identifier
unii: H0982HF78B
Primaquine PhosphatePRIMAQUINE PHOSPHATEUnichem Pharmaceuticals (USA), Inc.0c8c2bc6-428b-40b6-8114-6df80290878d2026-02-25Warnings, Adverse reactionsExact identifier
unii: H0982HF78B
Primaquine PhosphatePRIMAQUINE PHOSPHATESanofi-Aventis U.S. LLC1bfbf4ae-81b8-4160-a00d-6322aadd4b592026-02-11Warnings, Adverse reactionsExact identifier
unii: H0982HF78B

Reported adverse events (FAERS/openFDA)#

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