FDA.reportPublic FDA data

NDC 50989-327 - INSTAMAG

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
50989-327
Package NDCs from labels
50989-327-49
Manufacturer
Vedco, Inc.
Effective date
2022-11-15
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
INSTAMAG BOLUSVedco, Inc.2022-11-15OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50989-327-49INSTAMAG50 in 1 BOXTABLET507

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50989-327INSTAMAG (MAGNESIUM OXIDE) TABLET [VEDCO, INC.]71 package rows20221119_36bee200-d57e-4461-b99a-5ff7ca009448.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 4 of 4 · 72 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Vitrexate FEFERROUS FUMARATE, FOLIC ACIDPureTek Corporationb3637def-a701-673a-e053-2995a90a02d52023-01-11Warnings, Adverse reactionsExact identifier
unii: 3A3U0GI71G
VenexaFOLIC ACIDPureTek Corporationba130779-cdfd-086d-e053-2a95a90a25902023-01-11Warnings, Adverse reactionsExact identifier
unii: 3A3U0GI71G
Venexa FEFERROUS FUMARATE, FOLIC ACIDPureTek Corporationba142128-21c4-4204-e053-2a95a90ae0d72023-01-11Warnings, Adverse reactionsExact identifier
unii: 3A3U0GI71G
Ribotin-EFERROUS FUMARATE, FOLIC ACIDPureTek Corporationbb1492c5-bfcd-d632-e053-2a95a90ad7d12023-01-11Warnings, Adverse reactionsExact identifier
unii: 3A3U0GI71G
Ventrixyl FeFERROUS FUMARATE, FOLIC ACIDPureTek Corporationc7a626ec-88ec-d899-e053-2a95a90ab0ba2023-01-11Warnings, Adverse reactionsExact identifier
unii: 3A3U0GI71G
Zintrexyl-CFERROUS FUMARATE, FOLIC ACIDPureTek Corporationbb1492c5-bfca-d632-e053-2a95a90ad7d12023-01-11Warnings, Adverse reactionsExact identifier
unii: 3A3U0GI71G
Magnesia OxydataMAGNESIA OXYDATAHahnemann Laboratories, INC.e45bc2b0-72f4-42e1-e053-2995a90a0e662022-07-21Exact identifier
unii: 3A3U0GI71G
Magnesium OxideMAGNESIUM OXIDEEndo USAd5c123f8-1396-4d8c-96d3-e5ade96a6ef82020-11-10WarningsExact identifier
unii: 3A3U0GI71G
Magnesium OxideMAGNESIUM OXIDEEndo USAd3c5b01b-f0d6-4503-ab18-b1a72386e2c62020-06-03WarningsExact identifier
unii: 3A3U0GI71G
Magnesium Oxide 400mgMAGNESIUM OXIDE 400MGAllegiant Health2ea68874-8c20-4284-bd0a-f07768057b832019-01-28WarningsExact identifier
unii: 3A3U0GI71G
Magnesium OxideMAGNESIUM OXIDEAphena Pharma Solutions - Tennessee, LLC11b2ce71-61fd-4e75-a859-a260b1dda0802018-11-07WarningsExact identifier
unii: 3A3U0GI71G
Magnesium OxideMAGNESIUM OXIDEAphena Pharma Solutions - Tennessee, LLCedabc9e4-60ad-407f-97c8-dfec5ee7eeb12018-10-25WarningsExact identifier
unii: 3A3U0GI71G

Reported adverse events (FAERS/openFDA)#

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