FDA.reportPublic FDA data

NDC 0009-0193 - 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
0009-0193
Package NDCs from labels
0009-0193-01, 0009-0193-02
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
0009-0193-01Deltasone100 in 1 BOTTLETABLET1001
0009-0193-02Deltasone500 in 1 BOTTLETABLET5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0009-0193DELTASONE (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 11 of 12 · 229 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
prednisonePREDNISONEMedsource Pharmaceuticals131780a0-31f3-6588-e063-6294a90a2f8e2024-03-07Warnings, Adverse reactionsExact identifier
rxcui: 312615
PredniSONEPREDNISONENuCare Pharmaceuticals,Inc.1289c6d2-2707-baca-e063-6294a90a750d2024-02-29Warnings, Adverse reactionsExact identifier
rxcui: 312617
PrednisonePREDNISONEA-S Medication Solutions95cf05e5-1446-43f5-8447-c04877a747812024-02-27Warnings, Adverse reactionsExact identifier
rxcui: 198145
PREDNISONEPREDNISONEAurobindo Pharma Limitedb1ac4c92-e1fd-4015-b172-0932790ae0192024-02-16Warnings, Adverse reactionsExact identifier
rxcui: 198145
rxcui: 198146
rxcui: 312615
rxcui: 198148
rxcui: 312617
PrednisonePREDNISONEA-S Medication Solutions410988ea-456a-454e-932c-fcbdbef04ba92024-01-18Warnings, Adverse reactionsExact identifier
rxcui: 198145
PrednisonePREDNISONEA-S Medication Solutions44069d49-4cf4-4f1e-9fbd-b496c6ca81a12024-01-18Warnings, Adverse reactionsExact identifier
rxcui: 198145
prednisonePREDNISONEA-S Medication Solutions17278e0a-cbff-4a95-96ee-f34f7466faa02023-11-24Warnings, Adverse reactionsExact identifier
rxcui: 312617
PrednisonePREDNISONEChartwell RX, LLC92483276-d55c-42c6-8bbc-27137ff252962023-09-06Warnings, Adverse reactionsExact identifier
rxcui: 312615
prednisonePREDNISONEProficient Rx LP6a0c1192-8ce4-466d-a0f3-d878d67349cf2023-09-01Warnings, Adverse reactionsExact identifier
rxcui: 312615
PrednisonePREDNISONEProficient Rx LP5961b1d4-6a4c-452f-b3f1-c99f3a9a64452023-09-01Warnings, Adverse reactionsExact identifier
rxcui: 198145
PredniSONEPREDNISONEA-S Medication Solutions0060b86b-0b79-4c54-a7be-97683a933a052023-08-31Warnings, Adverse reactionsExact identifier
rxcui: 312617
PredniSONEPREDNISONEA-S Medication Solutionsf11c190e-edf8-454d-82c4-1ed769b5a6d22023-08-31Warnings, Adverse reactionsExact identifier
rxcui: 312617
PredniSONEPREDNISONEA-S Medication Solutions6f0719a2-1759-4354-9363-bb9fb3bddb3d2023-08-31Warnings, Adverse reactionsExact identifier
rxcui: 312617
prednisonePREDNISONEProficient Rx LP6ec5b58c-65e9-47ee-b2ac-7d0b395a06302023-07-01Warnings, Adverse reactionsExact identifier
rxcui: 198145
prednisonePREDNISONEProficient Rx LP22d9fd96-cad5-4762-9a56-0ff63357ed9e2023-02-01Warnings, Adverse reactionsExact identifier
rxcui: 198148
prednisonePREDNISONENCS HealthCare of KY, LLC dba Vangard Labsbc37cc2e-2f6a-4131-bb6a-63b6e576df212022-11-11Warnings, Adverse reactionsExact identifier
rxcui: 312617
PrednisonePREDNISONEPharmPak, Inc.03aaf69f-d9c7-433c-baea-9c6eca0fe1e52022-10-08Warnings, Adverse reactionsExact identifier
rxcui: 198145
PrednisonePREDNISONEProficient Rx LP71d70ec6-859a-4951-af98-248a864e11352022-09-01Warnings, Adverse reactionsExact identifier
rxcui: 198145
PredniSONEPREDNISONEProficient Rx LPe109f428-ca85-4a2c-acd0-ca8d498e77232022-06-01Warnings, Adverse reactionsExact identifier
rxcui: 198148
PrednisonePREDNISONEProficient Rx LP67681e4e-3002-4428-af5e-6ff1a950b0372022-05-02Warnings, Adverse reactionsExact identifier
rxcui: 312615

Reported adverse events (FAERS/openFDA)#

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