FDA.reportPublic FDA data

NDC 70069-021-01 - Dexamethasone Sodium 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
70069-021
Requested NDC
70069-021-01
Package NDCs from labels
70069-021-01, 70069-021-25
Manufacturer
Advanced Rx Pharmacy of Tennessee, LLC
Effective date
2024-12-31
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Dexamethasone Sodium Phosphate - Advanced Rx Pharmacy of Tennessee, LLCAdvanced Rx Pharmacy of Tennessee, LLC2024-12-31HUMAN PRESCRIPTION DRUG LABEL
DEXAMETHASONE - Somerset Therapeutics, LLC | Somerset Therapeutics Private Limited | Maiva Pharma Private LimitedSomerset Therapeutics, LLC | Somerset Therapeutics Private Limited | Maiva Pharma Private Limited2024-12-19HUMAN PRESCRIPTION DRUG LABEL
Dexamethasone Sodium Phosphate - REMEDYREPACK INC.REMEDYREPACK INC.2024-02-23HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70069-021-01Dexamethasone Sodium Phosphate1 mL in 1 VIALINJECTION19
70069-021-25Dexamethasone Sodium Phosphate25 in 1 CARTONINJECTION259

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70069-021DEXAMETHASONE SODIUM PHOSPHATE INJECTION [SOMERSET THERAPEUTICS, LLC]9Current NDC, Legacy NDC, 2 package rows20241222_799028e2-c0e4-494f-89ff-1b786babc34a.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70069-021-01ML - Milliliter70069-0216be3941d-983d-49d6-921a-12b726db9f9e12018-05-09
70069-021-25ML - Milliliter70069-0210fbdd5e7-fa9d-45ba-8bd6-51318bf5813512018-05-09

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 11 of 17 · 324 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
2174c952-bc01-64a2-e063-6294a90ae45e72c513e9-448d-4654-8e51-0ef156081ce82024-09-06Warnings, Adverse reactionsExact identifier
spl set id: 72c513e9-448d-4654-8e51-0ef156081ce8
Dexamethasone Sodium PhosphateDEXAMETHASONE SODIUM PHOSPHATEAmneal Pharmaceuticals LLCddc82c42-2e6e-42a6-a30a-e41978e2f4da2024-08-14Warnings, Adverse reactionsExact identifier
unii: AI9376Y64P
EmpathyAETHUSA CYNAPIUM, AMBRA GRISEA, ARGEMONE MEXICANA, CANDIDA ALBICANS, CARLSBAD AQUA, CEREBRUM SUIS, COCCULUS INDICUS, COFFEA TOSTA, CROCUS SATIVUS, CYCLAMEN EUROPAEUM, MAGNESIA CARBONICA, NATRUM CARBONICUM, NUPHAR LUTEUM, NUX MOSCHATA, PHOSPHORUS, PLACENTA TOTALIS SUIS, ROSA DAMASCENA, SUCCINUM, VIOLA ODORATADeseret Biologicals, Inc.a89067c1-ef12-49da-8fa6-e65ff664f4972024-08-13WarningsExact identifier
unii: 059QF0KO0R
Dexamethasone Sodium PhosphateDEXAMETHASONE SODIUM PHOSPHATEAmneal Pharmaceuticals LLCba18ba23-9ea3-4ce1-84ae-74e9151bb6a42024-07-29Warnings, Adverse reactionsExact identifier
rxcui: 1812079
unii: AI9376Y64P
Thompson Safety EyewashWATERThompson Safety1d0e96cf-245b-cfb7-e063-6294a90a4ced2024-07-12WarningsExact identifier
unii: 059QF0KO0R
Dexamethasone Sodium PhosphateDEXAMETHASONE SODIUM PHOSPHATEGland Pharma Limitedc9d9ab76-6bc6-433d-aad7-8d49064ed7452024-06-26Warnings, Adverse reactionsExact identifier
rxcui: 1812079
unii: AI9376Y64P
Dexamethasone Sodium PhosphateDEXAMETHASONE SODIUM PHOSPHATEPhlow Corporation02d25ab8-8f51-452b-b944-f569fbae36fe2024-06-25Warnings, Adverse reactionsExact identifier
unii: AI9376Y64P
Eyesaline Emergency EyewashPURIFIED WATERHoneywell Safety Products USA, Inc.ad42a7e3-84ea-390d-e053-2a95a90a3a322024-06-14WarningsExact identifier
unii: 059QF0KO0R
Eyes Alive Eye WashWATERRIVIERA PHARMA INC081079f4-1c06-4054-b771-00fedaa666f62024-06-05WarningsExact identifier
unii: 059QF0KO0R
Sodium Citrate and Citric AcidSODIUM CITRATE AND CITRIC ACIDChartwell RX, LLC525136c9-7758-437b-b57b-94b9057868252024-05-31Adverse reactionsExact identifier
unii: 2968PHW8QP
Sterile WaterWATERBecton Dickinson and Company6e43c5a3-dad2-49ed-b500-964cb4563cc92024-05-31Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
DEXAMETHASONE SODIUM PHOSPHATEDEXAMETHASONE SODIUM PHOSPHATEHF Acquisition Co LLC, DBA HealthFirst18a70010-6cc5-19e2-e063-6394a90a0ea62024-05-28Warnings, Adverse reactionsExact identifier
unii: AI9376Y64P
PEMF OptimizerAQUA SULIS, ARGENTUM METALLICUM, AURUM METALLICUM, CUPRUM METALLICUM, LAPIS ALBUS, MANGANUM METALLICUM VANADIUM METALLICUM VISCUM ALBUM, ZINCUM METALLICUMDeseret Biologicals, Inc.97d57469-4c5b-4d3f-9398-3a1a6617a6492024-04-23WarningsExact identifier
unii: 059QF0KO0R
Dexamethasone Sodium PhosphateDEXAMETHASONE SODIUM PHOSPHATEA-S Medication Solutionsd21f3055-8a8a-4797-93e2-c8f582cbdae12024-04-11Warnings, Adverse reactionsExact identifier
unii: AI9376Y64P
Sterile WaterWATERHikma Pharmaceuticals USA Inc.78ef7ad3-451d-43d0-a9b6-5cf0aadca0032024-04-10Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Sterile WaterWATERB. Braun Medical Inc.8fc8d87a-3951-4ac5-97df-c161ffc904752024-04-10Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
ANTICOAGULANT SODIUM CITRATETRISODIUM CITRATE DIHYDRATEBaxter Healthcare Corporation7025a0f9-1a56-4416-a3a4-925d755aed902024-04-02Exact identifier
unii: B22547B95K
Eye WashWATERM-star (Hubei) Health&Care Products Co., Ltd.71706039-e250-4f08-9687-71b2928c4e462024-04-01WarningsExact identifier
unii: 059QF0KO0R
ULINE EyewashEYEWASHUline.14545fc9-1fb4-befa-e063-6294a90a04742024-03-23WarningsExact identifier
unii: 059QF0KO0R
Dexamethasone Sodium PhosphateDEXAMETHASONE SODIUM PHOSPHATEMylan Institutional LLCdff598e8-e662-411f-978d-4ba3fb8ef7db2024-03-05Warnings, Adverse reactionsExact identifier
unii: AI9376Y64P

Reported adverse events (FAERS/openFDA)#

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