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 9 of 17 · 324 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Soothe ChewableCITRIC ACIDCarolina Cannabis Creations LLC04a7720f-1e74-7578-e063-6394a90a5eae2025-01-15WarningsExact identifier
unii: 2968PHW8QP
Soothe ChewableCITRIC ACIDCarolina Cannabis Creations LLC04a78060-7f0d-c4bd-e063-6294a90ae1522025-01-15WarningsExact identifier
unii: 2968PHW8QP
Soothe ChewableCITRIC ACIDCarolina Cannabis Creations LLC04a78a5c-e3b5-f362-e063-6394a90a08072025-01-15WarningsExact identifier
unii: 2968PHW8QP
D-99ATROPA BELLADONNA, NITROGLYCERIN, LACTIC ACID, UNSPECIFIED FORM, SCROPHULARIA NODOSA, ALOE, RADIUM BROMIDE, POTASSIUM IODIDE, SUS SCROFA BONE MARROW, ZINC, AND CITRIC ACID MONOHYDRATEDNA Labs, Inc.dd9c0226-35ea-445a-a570-1ec35551f68d2025-01-13WarningsExact identifier
unii: 2968PHW8QP
D-97ALUMINUM OXIDE, SILVER, SILVER NITRATE, ARSENIC TRIOXIDE, MERCURIUS SOLUBILIS, CALOMEL, MERCURIC IODIDE, LEAD, LEAD IODIDE, CHELIDONIUM MAJUS, ZINC, SOLIDAGO VIRGAUREA FLOWERING TOP, AND CITRIC ACID MONOHYDRATEDNA Labs, Inc.b2079abb-786c-4f92-8d49-5606c77f7d722025-01-13WarningsExact identifier
unii: 2968PHW8QP
STERILE WATERSTERILE WATERHF Acquisition Co. LLC, DBA HealthFirst74ed2a6f-824c-a1ff-e053-2a91aa0a57c02025-01-09Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
STERILE WATERSTERILE WATERHF Acquisition Co LLC, DBA HealthFirst77bd3c0f-f4ab-7cfa-e053-2a91aa0a1b832025-01-09Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
STERILE WATERSTERILE WATERHF Acquisition Co LLC, DBA HealthFirst7610bf80-61b7-982f-e053-2a91aa0ac1bb2025-01-09Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
T-27WATERDNA Labs, Inc.f0e9afd7-64a4-4b85-9c5f-4bf07ba4b4812025-01-09WarningsExact identifier
unii: 059QF0KO0R
Dexamethasone Sodium PhosphateDEXAMETHASONE SODIUM PHOSPHATEA-S Medication Solutions3c05089c-5a25-40c3-9abc-b2e40696bcdc2025-01-09Warnings, Adverse reactionsExact identifier
unii: AI9376Y64P
Dexamethasone Sodium PhosphateDEXAMETHASONE SODIUM PHOSPHATESomerset Therapeutics, LLC2dcbf312-6f4b-439a-8e2f-dda61eeb2cab2025-01-09Warnings, Adverse reactionsExact identifier
unii: AI9376Y64P
DEXAMETHASONE SODIUM PHOSPHATEDEXAMETHASONE SODIUM PHOSPHATEHF Acquisition Co LLC, DBA HealthFirst9a426a16-19f8-567e-e053-2a95a90a0a5b2025-01-08Warnings, Adverse reactionsExact identifier
unii: AI9376Y64P
Sterile WaterSTERILE WATER FOR INJECTIONMedefil, Inc.99e99a50-82d5-aff6-e053-2a95a90a8c562025-01-08Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
BACTERIOSTATIC WATERBACTERIOSTATIC WATERHF Acquisition Co LLC, DBA HealthFirst99b0ef9b-600a-40dc-e053-2a95a90aa07e2025-01-08Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
STERILE WATERSTERILE WATERHF Acquisition Co LLC, DBA HealthFirst99b1cb12-0b2d-0c0f-e053-2a95a90ac3b62025-01-08Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Emetrol Powder Non-DrowsySODIUM CITRATE DIHYDRATEWellSpring Pharmaceutical Corporation9d8d2ee7-9db7-4be7-8c73-511eb2e324592025-01-08WarningsExact identifier
unii: B22547B95K
DoubleDex KitDEXAMETHASONE SODIUM PHOSPHATE, POVIDINE IODINEAdvanced Rx Pharmacy of Tennessee, LLCfb85dd2c-6c90-6249-e053-6294a90a09fa2024-12-31Warnings, Adverse reactionsExact identifier
rxcui: 1812079
Dexamethasone Sodium PhosphateDEXAMETHASONE SODIUM PHOSPHATEAdvanced Rx Pharmacy of Tennessee, LLCf4d6c7c8-7a77-6a46-e053-2995a90a44112024-12-31Warnings, Adverse reactionsExact identifier
application number: ANDA207442
ndc (package): 80425-0261-1
ndc (product): 80425-0261
rxcui: 1812079
spl id: 2a9bad62-b2fd-697c-e063-6294a90aa395
spl set id: f4d6c7c8-7a77-6a46-e053-2995a90a4411
unii: AI9376Y64P
Dexamethasone Sodium PhosphateDEXAMETHASONE SODIUM PHOSPHATECivica, Inc.d54a27f2-2af8-4f86-a7fd-453f6b1a99972024-12-26Warnings, Adverse reactionsExact identifier
unii: AI9376Y64P
Dexamethasone Sodium PhosphateDEXAMETHASONE SODIUM PHOSPHATESomerset Therapeutics, LLC799028e2-c0e4-494f-89ff-1b786babc34a2024-12-19Warnings, Adverse reactionsExact identifier
application number: ANDA207442
ndc (package): 70069-021-01
ndc (package): 70069-021-25
ndc (product): 70069-021
ndc11 (package): 70069002101
rxcui: 1812079
spl id: 73618326-ff56-4a30-9d6d-6b019b61c2cd
spl set id: 799028e2-c0e4-494f-89ff-1b786babc34a
unii: AI9376Y64P

Reported adverse events (FAERS/openFDA)#

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