FDA.reportPublic FDA data

NDC 0009-0165 - Deltasone

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
0009-0165
Package NDCs from labels
0009-0165-01, 0009-0165-02
Manufacturer
Pharmacia and Upjohn and Company
Effective date
2007-03-30
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Deltasone - Pharmacia and Upjohn and CompanyPharmacia and Upjohn and Company2007-03-30HUMAN PRESCRIPTION DRUG LABELING

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0009-0165-01Deltasone100 in 1 BOTTLETABLET1001
0009-0165-02Deltasone500 in 1 BOTTLETABLET5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0009-0165DELTASONE (PREDNISONE) TABLET [PHARMACIA AND UPJOHN AND COMPANY]12 package rows20070426_3400D26A-41CB-40E4-99B4-780E1E0EC561.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
PrednisoneACTIVE INGREDIENTVB0R961HZTDELTASONE (PREDNISONE) TABLET [PHARMACIA AND UPJOHN AND COMPANY]1
PrednisoneACTIVE MOIETYVB0R961HZTDELTASONE (PREDNISONE) TABLET [PHARMACIA AND UPJOHN AND COMPANY]1
calcium stearateINACTIVE INGREDIENT776XM7047LDELTASONE (PREDNISONE) TABLET [PHARMACIA AND UPJOHN AND COMPANY]1
corn starchINACTIVE INGREDIENTDELTASONE (PREDNISONE) TABLET [PHARMACIA AND UPJOHN AND COMPANY]1
erythrosine sodiumINACTIVE INGREDIENTDELTASONE (PREDNISONE) TABLET [PHARMACIA AND UPJOHN AND COMPANY]1
FD&C yellow no.6INACTIVE INGREDIENTDELTASONE (PREDNISONE) TABLET [PHARMACIA AND UPJOHN AND COMPANY]1
lactoseINACTIVE INGREDIENTDELTASONE (PREDNISONE) TABLET [PHARMACIA AND UPJOHN AND COMPANY]1
magnesium stearateINACTIVE INGREDIENT70097M6I30DELTASONE (PREDNISONE) TABLET [PHARMACIA AND UPJOHN AND COMPANY]1
mineral oilINACTIVE INGREDIENTDELTASONE (PREDNISONE) TABLET [PHARMACIA AND UPJOHN AND COMPANY]1
sorbic acidINACTIVE INGREDIENTX045WJ989BDELTASONE (PREDNISONE) TABLET [PHARMACIA AND UPJOHN AND COMPANY]1
sucroseINACTIVE INGREDIENTC151H8M554DELTASONE (PREDNISONE) TABLET [PHARMACIA AND UPJOHN AND COMPANY]1
talcINACTIVE INGREDIENT7SEV7J4R1UDELTASONE (PREDNISONE) TABLET [PHARMACIA AND UPJOHN AND COMPANY]1

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 6 of 12 · 229 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
PredniSONEPREDNISONENorthwind Health Company, LLCc9f4711d-319c-d952-e053-2a95a90a36972026-01-01Warnings, Adverse reactionsExact identifier
rxcui: 198145
prednisonePREDNISONENorthwind Health Company, LLCfc4cd6f4-e01f-ad2d-e053-6294a90aebd62026-01-01Warnings, Adverse reactionsExact identifier
rxcui: 312615
prednisonePREDNISONERedpharm Drug0ab0e81c-8170-6805-e063-6294a90adfc02025-12-25Warnings, Adverse reactionsExact identifier
rxcui: 312615
PrednisonePREDNISONEAmerican Health Packaginga0e8d1a2-8c82-4dc0-8c2f-9da84382f34e2025-12-23Warnings, Adverse reactionsExact identifier
rxcui: 198145
rxcui: 312615
rxcui: 312617
prednisonePREDNISONEA-S Medication Solutionse28359cf-0c21-487a-a1a3-d1c62cef88f92025-12-23Warnings, Adverse reactionsExact identifier
rxcui: 312615
PREDNISONEPREDNISONEA-S Medication Solutions35de14e3-d748-46bd-a307-6a1a27c626a22025-12-17Warnings, Adverse reactionsExact identifier
rxcui: 198146
prednisonePREDNISONEStrides Pharma Science Limited2ef05381-faad-4e0f-b58d-9f2236a04a2c2025-12-15Warnings, Adverse reactionsExact identifier
rxcui: 198145
rxcui: 312615
rxcui: 198148
PREDNISONEPREDNISONERedpharm Drug44f5e966-5a12-e2ff-e063-6294a90a919e2025-12-13Warnings, Adverse reactionsExact identifier
rxcui: 312615
PrednisonePREDNISONEChartwell RX, LLC36631112-3abb-4003-886b-9fe6d9cbe2cc2025-12-11Warnings, Adverse reactionsExact identifier
rxcui: 312617
prednisonePREDNISONEStrides Pharma Science Limited52010a34-aadb-4561-ac4a-3ee53f5e35662025-12-10Warnings, Adverse reactionsExact identifier
rxcui: 198146
rxcui: 312617
PredniSONEPREDNISONEQPharma, Inc.318fdf0d-c03a-4b48-a380-b7bb630363fb2025-12-05Warnings, Adverse reactionsExact identifier
rxcui: 198145
PrednisonePREDNISONEQPharma, Inc.07fb8daa-2ceb-4564-b0d0-6cdf903da0b52025-12-03Warnings, Adverse reactionsExact identifier
rxcui: 198145
PrednisonePREDNISONEQPharma, Inc.f4d5974a-444f-4ef0-84a9-803150ccdeac2025-12-03Warnings, Adverse reactionsExact identifier
rxcui: 312617
PrednisonePREDNISONEQPharma, Inc.d898d53f-c7d2-4bdb-bd9e-5f200070d1232025-12-03Warnings, Adverse reactionsExact identifier
rxcui: 312615
PredniSONE Tablets, USP, 5 mgPREDNISONEBryant Ranch Prepack475c6480-2a6a-4698-aff3-7affb154f2a72025-12-03Warnings, Adverse reactionsExact identifier
rxcui: 312617
PredniSONE Tablets, USP, 20 mgPREDNISONEBryant Ranch Prepack0e55a02d-2de4-42c4-adc2-49536b8992252025-12-03Warnings, Adverse reactionsExact identifier
rxcui: 312615
PredniSONE Tablets, USP, 10 mgPREDNISONEBryant Ranch Prepack61dab6c2-4019-4d7c-bc8b-3a0a463beefc2025-12-03Warnings, Adverse reactionsExact identifier
rxcui: 198145
PredniSONE Tablets, USP, 20 mgPREDNISONEBryant Ranch Prepack53bd04e8-6cbd-45f6-ac59-53fd3005a2212025-12-03Warnings, Adverse reactionsExact identifier
rxcui: 312615
PredniSONE Tablets, USP, 10 mgPREDNISONEBryant Ranch Prepack8520622e-c0e3-4226-be84-e332ab98e6a72025-12-03Warnings, Adverse reactionsExact identifier
rxcui: 198145
PredniSONE Tablets, USP, 5 mgPREDNISONEBryant Ranch Prepack5e5c81bf-7cbb-4f02-b107-16efe3d353ee2025-12-03Warnings, Adverse reactionsExact identifier
rxcui: 312617

Reported adverse events (FAERS/openFDA)#

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