FDA.reportPublic FDA data

NDC 0998-0635-10 - Econopred

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
0998-0635
Requested NDC
0998-0635-10
Package NDCs from labels
0998-0635-05, 0998-0635-10
Manufacturer
Alcon Laboratories, Inc.
Effective date
2006-09-11
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Econopred - Alcon Laboratories, Inc.Alcon Laboratories, Inc.2006-09-11Human Prescription Drug Label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0998-0635-05Econopred5 mL in 1 BOTTLE, PLASTICSUSPENSION51
0998-0635-10Econopred10 mL in 1 BOTTLE, PLASTICSUSPENSION101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0998-0635ECONOPRED (PREDNISOLONE ACETATE) SUSPENSION [ALCON LABORATORIES, INC.]12 package rows20080313_2d6c3ea4-5189-4f6e-bb6a-c9379f441d7a.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
prednisolone acetateACTIVE INGREDIENT8B2807733DECONOPRED (PREDNISOLONE ACETATE) SUSPENSION [ALCON LABORATORIES, INC.]1
prednisoloneACTIVE MOIETY9PHQ9Y1OLMECONOPRED (PREDNISOLONE ACETATE) SUSPENSION [ALCON LABORATORIES, INC.]1
benzalkonium chlorideINACTIVE INGREDIENTECONOPRED (PREDNISOLONE ACETATE) SUSPENSION [ALCON LABORATORIES, INC.]1
citric acid and/or sodium hydroxideINACTIVE INGREDIENTECONOPRED (PREDNISOLONE ACETATE) SUSPENSION [ALCON LABORATORIES, INC.]1
dibasic sodium phosphateINACTIVE INGREDIENTGR686LBA74ECONOPRED (PREDNISOLONE ACETATE) SUSPENSION [ALCON LABORATORIES, INC.]1
edetate disodiumINACTIVE INGREDIENT7FLD91C86KECONOPRED (PREDNISOLONE ACETATE) SUSPENSION [ALCON LABORATORIES, INC.]1
glycerinINACTIVE INGREDIENTPDC6A3C0OXECONOPRED (PREDNISOLONE ACETATE) SUSPENSION [ALCON LABORATORIES, INC.]1
hydroxypropyl methylcelluloseINACTIVE INGREDIENTECONOPRED (PREDNISOLONE ACETATE) SUSPENSION [ALCON LABORATORIES, INC.]1
polysorbate 80INACTIVE INGREDIENTECONOPRED (PREDNISOLONE ACETATE) SUSPENSION [ALCON LABORATORIES, INC.]1
waterINACTIVE INGREDIENT059QF0KO0RECONOPRED (PREDNISOLONE ACETATE) SUSPENSION [ALCON LABORATORIES, INC.]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 1 of 1 ยท 15 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
PREDNISOLONE ACETATEPREDNISOLONE ACETATEA-S Medication Solutionsdd32d625-fb2f-4c51-89fe-cdccdf0201b92026-08-03Warnings, Adverse reactionsExact identifier
rxcui: 1376336
Prednisolone AcetatePREDNISOLONE ACETATESportpharm LLC3011a244-24a4-46ef-979a-b5d9e70762462026-07-23Warnings, Adverse reactionsExact identifier
rxcui: 1376336
PREDNISOLONE ACETATEPREDNISOLONE ACETATESportpharm LLC02fc6f0b-d053-49e1-82de-f272dd05d5292026-04-24Warnings, Adverse reactionsExact identifier
rxcui: 1376336
PREDNISOLONE ACETATEPREDNISOLONE ACETATEA-S Medication Solutionsf0e1b691-73ff-49ee-8a3c-71769b284ab82026-03-03Warnings, Adverse reactionsExact identifier
rxcui: 1376336
PREDNISOLONE ACETATEPREDNISOLONE ACETATERedpharm Drug3dd0195c-8522-bbf9-e063-6394a90a9f3e2025-12-02Warnings, Adverse reactionsExact identifier
rxcui: 1376336
PREDNISOLONE ACETATEPREDNISOLONE ACETATELupin Pharmaceuticals, Inc.75fbeab1-ce8d-4999-a875-472174be5cc62025-10-13Warnings, Adverse reactionsExact identifier
rxcui: 1376336
prednisolone acetatePREDNISOLONE ACETATEAmneal Pharmaceuticals NY LLC8d8e8f9b-4d65-426f-8c57-451001cdd8492025-06-12Warnings, Adverse reactionsExact identifier
rxcui: 1376336
STRENZA PLUSMOXIFLOXACIN 0.5%, BROMFENAC 0.09%, PREDNISOLONE ACETATE 1%Brisk Pharmaceuticals2df9064c-0527-4c21-e063-6294a90a56d82025-02-12Exact identifier
rxcui: 1376336
Prednisolone AcetatePREDNISOLONE ACETATESandoz Inc05d205c7-8f51-46b9-a6c5-4199bc432b262024-12-30Warnings, Adverse reactionsExact identifier
rxcui: 1376336
PREDNISOLONE ACETATEPREDNISOLONE ACETATEA-S Medication Solutions388abc87-cd5a-4e88-8675-7bf0c5ce7af52024-10-14Warnings, Adverse reactionsExact identifier
rxcui: 1376336
PREDNISOLONE ACETATEPREDNISOLONE ACETATENuCare Pharmaceuticals,Inc.ab72cf3d-7660-41b1-e053-2995a90a7f442024-07-17Warnings, Adverse reactionsExact identifier
rxcui: 1376336
PREDNISOLONE ACETATEPREDNISOLONE ACETATEPacific Pharma, Inc.1474d1df-70b6-4b1e-86d1-3349aa6d42fb2024-03-19Warnings, Adverse reactionsExact identifier
rxcui: 1376336
PRED FORTEPREDNISOLONE ACETATEAllergan, Inc.00a5aa88-e361-4ea7-8922-530c738b726e2024-02-02Warnings, Adverse reactionsExact identifier
rxcui: 1376336
Prednisolone AcetatePREDNISOLONE ACETATEA-S Medication Solutionsb1d30a4f-4941-45a5-bd24-fea07f1bfc872023-04-30Warnings, Adverse reactionsExact identifier
rxcui: 1376336
PREDNISOLONE ACETATEPREDNISOLONE ACETATEAsclemed USA, Inc.232e40a5-17c5-4cf3-9e3b-110a194ad4be2021-11-30Warnings, Adverse reactionsExact identifier
rxcui: 1376336

Reported adverse events (FAERS/openFDA)#

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