FDA.reportPublic FDA data

NDC 60219-1706-01 - 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
60219-1706
Requested NDC
60219-1706-01
Package NDCs from labels
60219-1706-1, 60219-1706-7, 60219-1706-2, 60219-1706-3, 60219-1706-01
Manufacturer
Amneal Pharmaceuticals NY LLC
Effective date
2026-04-14
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
prednisone - Amneal Pharmaceuticals NY LLCAmneal Pharmaceuticals NY LLC2026-04-14HUMAN PRESCRIPTION DRUG LABEL
prednisone - Northwind Health Company, LLCNorthwind Health Company, LLC2026-01-01HUMAN PRESCRIPTION DRUG LABEL
prednisone - A-S Medication SolutionsA-S Medication Solutions2025-10-12HUMAN PRESCRIPTION DRUG LABEL
prednisone - A-S Medication SolutionsA-S Medication Solutions2025-10-12HUMAN PRESCRIPTION DRUG LABEL
prednisone - A-S Medication SolutionsA-S Medication Solutions2025-10-12HUMAN PRESCRIPTION DRUG LABEL
prednisone - Coupler LLCCoupler LLC2024-11-11HUMAN PRESCRIPTION DRUG LABEL
PredniSONE Tablets, USP (1 mg and 5 mg) Rx onlyPreferred Pharmaceuticals Inc.2024-07-31HUMAN PRESCRIPTION DRUG LABEL
prednisone - NCS HealthCare of KY, LLC dba Vangard LabsNCS HealthCare of KY, LLC dba Vangard Labs2022-11-11HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60219-1706-1prednisone100 in 1 BOTTLE, PLASTICTABLET10014
60219-1706-2prednisone10 in 1 BLISTER PACKTABLET1014
60219-1706-3prednisone10 in 1 CARTONTABLET1014
60219-1706-7prednisone1000 in 1 BOTTLE, PLASTICTABLET100014

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60219-1706PREDNISONE TABLET [AMNEAL PHARMACEUTICALS NY LLC]13Current NDC, Legacy NDC, 4 package rows20240922_0740ef68-7641-432e-bd46-4710687fc9d7.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
60219-1706-1EA - Each60219-1706a60ee825-64af-4e0f-9190-306f6275ee1d12021-11-09
60219-1706-7EA - Each60219-1706381b20d4-18d0-42ff-8f8a-fb95d4a3bf4612021-11-09

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 7 of 13 · 248 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
PrednisonePREDNISONEQPharma, Inc.f4d5974a-444f-4ef0-84a9-803150ccdeac2025-12-03Warnings, Adverse reactionsExact identifier
rxcui: 312617
unii: VB0R961HZT
PrednisonePREDNISONEQPharma, Inc.d898d53f-c7d2-4bdb-bd9e-5f200070d1232025-12-03Warnings, Adverse reactionsExact identifier
unii: VB0R961HZT
PredniSONE Tablets, USP, 5 mgPREDNISONEBryant Ranch Prepack475c6480-2a6a-4698-aff3-7affb154f2a72025-12-03Warnings, Adverse reactionsExact identifier
rxcui: 312617
unii: VB0R961HZT
prednisonePREDNISONEStrides Pharma Science Limiteda2c2e8ee-d222-47c5-93c2-8b44160a7e482025-12-03Warnings, Adverse reactionsExact identifier
rxcui: 198144
unii: VB0R961HZT
PredniSONE Tablets, USP, 20 mgPREDNISONEBryant Ranch Prepack0e55a02d-2de4-42c4-adc2-49536b8992252025-12-03Warnings, Adverse reactionsExact identifier
unii: VB0R961HZT
PredniSONE Tablets, USP, 10 mgPREDNISONEBryant Ranch Prepack61dab6c2-4019-4d7c-bc8b-3a0a463beefc2025-12-03Warnings, Adverse reactionsExact identifier
unii: VB0R961HZT
PredniSONE Tablets, USP, 20 mgPREDNISONEBryant Ranch Prepack53bd04e8-6cbd-45f6-ac59-53fd3005a2212025-12-03Warnings, Adverse reactionsExact identifier
unii: VB0R961HZT
PredniSONE Tablets, USP, 10 mgPREDNISONEBryant Ranch Prepack8520622e-c0e3-4226-be84-e332ab98e6a72025-12-03Warnings, Adverse reactionsExact identifier
unii: VB0R961HZT
PredniSONE Tablets, USP, 5 mgPREDNISONEBryant Ranch Prepack5e5c81bf-7cbb-4f02-b107-16efe3d353ee2025-12-03Warnings, Adverse reactionsExact identifier
rxcui: 312617
unii: VB0R961HZT
PrednisonePREDNISONEQPharma, Inc.c0e147a8-36a9-1e61-e053-2a95a90afd622025-12-01Warnings, Adverse reactionsExact identifier
rxcui: 312617
unii: VB0R961HZT
PrednisonePREDNISONEMarlex Pharmaceuticals, Inc.f499197b-b9b7-1707-e053-2a95a90a09322025-11-21Warnings, Adverse reactionsExact identifier
rxcui: 312617
unii: VB0R961HZT
prednisonePREDNISONEA-S Medication Solutions8f9a581c-5fef-4089-aa94-7dc81ec5b5662025-11-10Warnings, Adverse reactionsExact identifier
unii: VB0R961HZT
prednisonePREDNISONEA-S Medication Solutions871540d3-39c3-460c-a855-3aeabfd872672025-11-10Warnings, Adverse reactionsExact identifier
unii: VB0R961HZT
PREDNISONEPREDNISONECoupler LLC41e6f1c3-d225-0ff0-e063-6394a90ace882025-10-24Warnings, Adverse reactionsExact identifier
unii: VB0R961HZT
PredniSONE Tablets, USP, 5 mgPREDNISONEBryant Ranch Prepack83e825cc-fb19-48b9-9f15-6aba6b1cef572025-10-20Warnings, Adverse reactionsExact identifier
rxcui: 312617
unii: VB0R961HZT
PredniSONEPREDNISONEPD-Rx Pharmaceuticals, Inc.5b2f4fa9-817c-43c9-ac9a-750ab1d1f66f2025-10-20Warnings, Adverse reactionsExact identifier
unii: VB0R961HZT
PREDNISONEPREDNISONEPD-Rx Pharmaceuticals, Inc.c21be016-6b25-4e09-b253-23b58884ccb62025-10-14Warnings, Adverse reactionsExact identifier
unii: VB0R961HZT
PrednisonePREDNISONEDirect_Rx24882e23-c05f-f2ee-e063-6294a90a536f2025-10-13Warnings, Adverse reactionsExact identifier
unii: VB0R961HZT
prednisonePREDNISONEA-S Medication Solutions80705a8a-f007-4a18-82a6-a73733d57ea22025-10-12Warnings, Adverse reactionsExact identifier
application number: ANDA213385
ndc (package): 50090-7688-0
ndc (product): 50090-7688
rxcui: 312617
spl id: 25a1ff72-3013-4b8b-b1b6-db0d65346ce0
spl set id: 80705a8a-f007-4a18-82a6-a73733d57ea2
unii: VB0R961HZT
prednisonePREDNISONEA-S Medication Solutions43a4b2eb-f2cd-410f-9719-577fdc4ad5de2025-10-12Warnings, Adverse reactionsExact identifier
application number: ANDA213385
ndc (package): 50090-7684-1
ndc (package): 50090-7684-0
ndc (package): 50090-7684-3
ndc (package): 50090-7684-7
ndc (package): 50090-7684-4
ndc (product): 50090-7684
rxcui: 312617
spl id: 4e631e86-7caf-4cad-8d38-f24c5d1d968b
spl set id: 43a4b2eb-f2cd-410f-9719-577fdc4ad5de
unii: VB0R961HZT

Reported adverse events (FAERS/openFDA)#

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