FDA.reportPublic FDA data

NDC 50090-3137-01 - 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
50090-3137
Requested NDC
50090-3137-01
Package NDCs from labels
50090-3137-0, 50090-3137-5, 50090-3137-7, 50090-3137-1, 50090-3137-4, 50090-3137-8, 50090-3137-2, 50090-3137-01
Manufacturer
A-S Medication Solutions
Effective date
2025-07-03
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Prednisone - A-S Medication SolutionsA-S Medication Solutions2025-07-03HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50090-3137-0Prednisone10 in 1 BOTTLETABLET1022
50090-3137-1Prednisone15 in 1 BOTTLETABLET1522
50090-3137-2Prednisone21 in 1 BOTTLETABLET2122
50090-3137-4Prednisone50 in 1 BOTTLETABLET5022
50090-3137-5Prednisone30 in 1 BOTTLETABLET3022
50090-3137-7Prednisone100 in 1 BOTTLETABLET10022
50090-3137-8Prednisone40 in 1 BOTTLETABLET4022

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50090-3137PREDNISONE (PREDNISONE) TABLET [A-S MEDICATION SOLUTIONS]19Current NDC, Legacy NDC, 7 package rows20240604_dc94273f-af06-4bd5-9ce3-ce0a0f36587b.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-3137-0EA - Each50090-3137a657058d-4baa-4a19-ad30-6768b205f92412021-09-07
50090-3137-1EA - Each50090-3137459ced8f-278f-46f1-8c35-b92884b0e58e12021-09-07
50090-3137-2EA - Each50090-3137913b705b-8c71-4689-9a3c-9a71f15fb54712019-05-02
50090-3137-4EA - Each50090-3137e77fd3e8-71fd-4201-978e-bc112def77eb12021-09-07
50090-3137-5EA - Each50090-31377b190702-04fe-496f-9858-078a269db30e12021-03-02
50090-3137-7EA - Each50090-313776d641e3-2e58-4ea6-ad47-fec5b3b3c53012021-09-07
50090-3137-8EA - Each50090-31370525e86b-f560-4afe-a4f1-bfbde4b4702d12023-08-08

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 3 of 17 · 336 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
prednisonePREDNISONEAmneal Pharmaceuticals NY LLC03228706-92b9-43c9-8d73-c73aa124c58d2026-06-30Warnings, Adverse reactionsExact identifier
rxcui: 198145
rxcui: 312615
unii: VB0R961HZT
PredniSONEPREDNISONESt. Mary's Medical Park Pharmacy16ee689e-c7a9-3a5a-e063-6394a90a6ea22026-06-22Warnings, Adverse reactionsExact identifier
unii: VB0R961HZT
prednisonePREDNISONESt. Mary's Medical Park Pharmacye4437eec-eadf-7c8b-e053-2a95a90af8462026-06-21Warnings, Adverse reactionsExact identifier
rxcui: 312615
unii: VB0R961HZT
PrednisonePREDNISONESt. Mary's Medical Park Pharmacy1b3ea4cc-5bc6-ae47-e063-6294a90af13d2026-06-15Warnings, Adverse reactionsExact identifier
rxcui: 312615
unii: VB0R961HZT
PrednisonePREDNISONERedpharm Drug5407a00b-1bfb-e37d-e063-6294a90a6c412026-06-12Warnings, Adverse reactionsExact identifier
rxcui: 198145
unii: VB0R961HZT
GUNA-BOWELALOE - ALUMINUM OXIDE - BRYONIA ALBA ROOT - CHELIDONIUM MAJUS - CHOLECALCIFEROL - COLLINSONIA - FRANGULA ALNUS BARK - NIACIN - PANTOTHENIC ACID - POTASSIUM CARBONATE - RHUBARB - SILYBUM MARIANUM SEED - SKATOLE - SODIUM CARBONATE - STRYCHNOS NUX-VOMICA SEED - SUS SCROFA COLON - SUS SCROFA RECTUM - TARAXACUM OFFICINALE - THIAMINE -Guna spa75465821-a889-4697-b470-e9588a5232052026-06-10WarningsExact identifier
unii: LMI26O6933
prednisonePREDNISONECoupler LLC53864d75-06ca-5c2a-e063-6394a90ad9662026-06-05Warnings, Adverse reactionsExact identifier
unii: VB0R961HZT
Borago NicotianaBORAGO NICOTIANAUriel Pharmacy Inc.306f9eee-877b-46ee-9a36-894fa321b3d32026-06-05WarningsExact identifier
unii: LMI26O6933
PredniSONE Tablets, USP, 20 mgPREDNISONEPD-Rx Pharmaceuticals, Inc.15230866-f547-47bf-ac7d-19afd6a41e2e2026-06-04Warnings, Adverse reactionsExact identifier
rxcui: 312615
unii: VB0R961HZT
PredniSONE Tablets, USP, 10 mgPREDNISONEPD-Rx Pharmaceuticals, Inc.bb32e309-e3c7-4009-bcd4-d97545b7e9752026-06-04Warnings, Adverse reactionsExact identifier
rxcui: 198145
unii: VB0R961HZT
PrednisonePREDNISONEA-S Medication Solutionsaaaa3460-0239-4203-857f-0ada303c21082026-06-01Warnings, Adverse reactionsExact identifier
rxcui: 312615
unii: VB0R961HZT
prednisonePREDNISONEBryant Ranch Prepackecc48869-3812-4440-a398-749b280620592026-05-29Warnings, Adverse reactionsExact identifier
rxcui: 198145
unii: VB0R961HZT
prednisonePREDNISONEBryant Ranch Prepack07d5e455-ac3b-4890-9619-609dd0be91062026-05-29Warnings, Adverse reactionsExact identifier
unii: VB0R961HZT
prednisonePREDNISONEAmerican Health Packagingfdcd49a6-6cb1-49f8-9f4c-feb475c129b32026-05-21Warnings, Adverse reactionsExact identifier
unii: VB0R961HZT
prednisonePREDNISONECardinal Health 107, LLC1d797f3e-a46c-42bc-91bb-c570ae8ca8c22026-05-20Warnings, Adverse reactionsExact identifier
unii: VB0R961HZT
prednisonePREDNISONEREMEDYREPACK INC.ea4070e1-080d-4feb-9561-3910c6b712dd2026-05-15Warnings, Adverse reactionsExact identifier
rxcui: 198145
unii: VB0R961HZT
PREDNISONEPREDNISONEST. MARY'S MEDICAL PARK PHARMACY42e0decc-4d11-e7e6-e063-6394a90a9fcc2026-05-14Warnings, Adverse reactionsExact identifier
rxcui: 312615
unii: VB0R961HZT
prednisonePREDNISONEREMEDYREPACK INC.b3b70d6f-dc44-4a54-b39b-2762f37d55752026-05-13Warnings, Adverse reactionsExact identifier
rxcui: 198145
unii: VB0R961HZT
prednisonePREDNISONEQPharma Inc11870c93-fe64-e6c9-e063-6394a90a53342026-05-11Warnings, Adverse reactionsExact identifier
unii: VB0R961HZT
prednisonePREDNISONEQPharma Incf795ea1d-f41a-6100-e053-6394a90a63a42026-05-11Warnings, Adverse reactionsExact identifier
rxcui: 198145
unii: VB0R961HZT

Reported adverse events (FAERS/openFDA)#

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