FDA.reportPublic FDA data

NDC 68788-8579-08 - prednisone

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
68788-8579
Requested NDC
68788-8579-08
Package NDCs from labels
68788-8579-8, 68788-8579-3, 68788-8579-08
Manufacturer
Preferred Pharmaceuticals Inc.
Effective date
2026-08-19
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
PredniSONE Tablets USP Rx onlyPreferred Pharmaceuticals Inc.2026-08-19HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68788-8579-3prednisone30 in 1 BOTTLE, PLASTICTABLET302
68788-8579-8prednisone21 in 1 BOTTLE, PLASTICTABLET212

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68788-8579PREDNISONE TABLET [PREFERRED PHARMACEUTICALS INC.]1Current NDC, 2 package rows20240306_fa75f5ce-8a74-4873-811f-7d9d9beec08f.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68788-8579-3EA - Each68788-8579926669a0-0ae2-4913-b88d-b36897cb1a3712024-05-16
68788-8579-8EA - Each68788-8579ceeca70d-321f-46d8-850f-4e68549cc55012024-05-16

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 13 · 252 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
PrednisonePREDNISONEBryant Ranch Prepack290a91e5-22ae-4d62-ab34-39a3117002e22026-09-08Warnings, Adverse reactionsExact identifier
rxcui: 312617
unii: VB0R961HZT
prednisonePREDNISONEREMEDYREPACK INC.4750028a-30ad-420a-8e6b-06dc2429d4332026-09-08Warnings, Adverse reactionsExact identifier
unii: VB0R961HZT
PrednisonePREDNISONEBryant Ranch Prepack0062fcc7-aa08-4990-9d33-d798725907f12026-09-08Warnings, Adverse reactionsExact identifier
unii: VB0R961HZT
PredniSONEPREDNISONEREMEDYREPACK INC.7db793b4-5768-4e9a-a47b-1ebbfed740012026-09-03Warnings, Adverse reactionsExact identifier
rxcui: 312617
unii: VB0R961HZT
PREDNISONEPREDNISONEREMEDYREPACK INC.0993b354-d936-472b-bafc-114f0f81bfb02026-09-01Warnings, Adverse reactionsExact identifier
unii: VB0R961HZT
PredniSONEPREDNISONEREMEDYREPACK INC.94715919-70bd-46c9-95fc-e151adf39cf92026-08-31Warnings, Adverse reactionsExact identifier
unii: VB0R961HZT
prednisonePREDNISONEREMEDYREPACK INC.23b12d22-97d6-426e-bf9c-dd6c2ff773702026-08-26Warnings, Adverse reactionsExact identifier
application number: ANDA208412
unii: VB0R961HZT
PredniSONE Tablets, USP, 20 mgPREDNISONEPD-Rx Pharmaceuticals, Inc.6b360c1f-c862-47ee-a40e-3903c2d6162f2026-08-21Warnings, Adverse reactionsExact identifier
unii: VB0R961HZT
PredniSONEPREDNISONEPreferred Pharmaceuticals Inc.02158832-550b-4855-a5c5-6abbf13ed6f02026-08-20Warnings, Adverse reactionsExact identifier
unii: VB0R961HZT
PrednisonePREDNISONEBryant Ranch Prepackc60a07f9-ed9f-4434-a69d-2e2fea4843fd2026-08-20Warnings, Adverse reactionsExact identifier
unii: VB0R961HZT
PrednisonePREDNISONEREMEDYREPACK INC.746b0bcd-122e-4ea8-a824-28415073a38e2026-08-20Warnings, Adverse reactionsExact identifier
rxcui: 312617
unii: VB0R961HZT
PrednisonePREDNISONEBryant Ranch Prepack7ea7f6a9-78ef-42fe-baac-f817da3976fb2026-08-20Warnings, Adverse reactionsExact identifier
rxcui: 312617
unii: VB0R961HZT
prednisonePREDNISONEPreferred Pharmaceuticals Inc.1e74ac55-4a48-4bf5-bfed-36c0fa37dd9f2026-08-19Warnings, Adverse reactionsExact identifier
application number: ANDA208412
unii: VB0R961HZT
prednisonePREDNISONEPreferred Pharmaceuticals Inc.fa75f5ce-8a74-4873-811f-7d9d9beec08f2026-08-19Warnings, Adverse reactionsExact identifier
application number: ANDA209727
ndc (package): 68788-8579-8
ndc (package): 68788-8579-3
ndc (product): 68788-8579
ndc11 (package): 68788857908
rxcui: 312617
spl id: 4a38efae-5e21-453b-9720-6ac049999f05
spl set id: fa75f5ce-8a74-4873-811f-7d9d9beec08f
unii: VB0R961HZT
prednisonePREDNISONEPreferred Pharmaceuticals Inc.930b5eea-3ec8-47df-a76d-1e0bc0b5c5b22026-08-19Warnings, Adverse reactionsExact identifier
application number: ANDA209727
rxcui: 198146
unii: VB0R961HZT
PrednisonePREDNISONEPreferred Pharmaceuticals, Inc.f89bd1dc-88cd-4aef-a7ae-6310f38a34232026-08-19Warnings, Adverse reactionsExact identifier
rxcui: 312617
unii: VB0R961HZT
PrednisonePREDNISONEMajor Pharmaceuticals57b98930-92ab-4b77-a033-ae9895ee718a2026-08-19Warnings, Adverse reactionsExact identifier
unii: VB0R961HZT
prednisonePREDNISONEPreferred Pharmaceuticals Inc.ce7663a7-4c91-4790-aa43-96f259b3bb182026-08-19Warnings, Adverse reactionsExact identifier
application number: ANDA208412
unii: VB0R961HZT
prednisonePREDNISONEREMEDYREPACK INC.e47a0448-331f-4846-8e63-c52c3afa274b2026-08-11Warnings, Adverse reactionsExact identifier
unii: VB0R961HZT
PrednisonePREDNISONECardinal Health 107, LLC568b8880-7997-4786-8c57-28816ce526552026-08-07Warnings, Adverse reactionsExact identifier
unii: VB0R961HZT

Reported adverse events (FAERS/openFDA)#

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