NDC 69375-003 - Ferrous Sulfate 324mg Enteric Coated

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
69375-003
Package NDCs from labels
69375-003-10
Manufacturer
Nationwide Pharmaceutical, LLC
Effective date
2024-10-11
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Ferrous Sulfate 324mg Enteric Coated - Nationwide Pharmaceutical, LLCNationwide Pharmaceutical, LLC2024-10-11DIETARY SUPPLEMENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69375-003-10Ferrous Sulfate 324mg Enteric Coated100 in 1 BOTTLETABLET, DELAYED RELEASE1002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69375-003FERROUS SULFATE 324MG ENTERIC COATED (FERROUS SULFATE) TABLET, DELAYED RELEASE [NATIONWIDE PHARMACEUTICAL, LLC]21 package rows20241024_3fbacc74-d2e6-459f-9b6e-1dbc49690fef.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
69375-003-10EA - Each69375-0036a67d892-12b8-40bf-a5a5-1e495c51911d12024-04-05

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 39 of 39 · 761 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
TeethingARNICA MONTANA, TRIFOLIUM PRATENSE, CALCAREA CARBONICA, CALCAREA FLUORICA, CALCAREA PHOSPHORICA, CHAMOMILLA, KREOSOTUM, SILICEABioActive Nutritional, Inc.f39c9feb-f567-43a2-a026-2a581aeeed9d2016-07-27WarningsExact identifier
unii: ETJ7Z6XBU4

Reported adverse events (FAERS/openFDA)#

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