FDA.reportPublic FDA data

NDC 71335-9703-01 - Fosinopril sodium

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
71335-9703
Requested NDC
71335-9703-01
Package NDCs from labels
71335-9703-1, 71335-9703-2, 71335-9703-3, 71335-9703-01
Manufacturer
Bryant Ranch Prepack
Effective date
2023-05-11
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Fosinopril sodium - Bryant Ranch PrepackBryant Ranch Prepack2023-05-11HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71335-9703-1Fosinopril sodium30 in 1 BOTTLETABLET30100
71335-9703-2Fosinopril sodium90 in 1 BOTTLETABLET90100
71335-9703-3Fosinopril sodium28 in 1 BOTTLETABLET28100

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71335-9703FOSINOPRIL SODIUM TABLET [BRYANT RANCH PREPACK]100Current NDC, 3 package rows20230525_ee78de8e-22f4-4c3b-a721-e9464d704eda.zip

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 14 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Fosinopril SodiumFOSINOPRIL SODIUMChartwell RX, LLCff1323cc-7ad8-488d-94a7-a11555db78a72025-10-10Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 857183
rxcui: 857187
rxcui: 857169
unii: NW2RTH6T2N
YVTYVT MICRODERMABRASION FACIAL SCRUBYVTYVT MICRODERMABRASION FACIAL SCRUBBeijing JUNGE Technology Co., Ltd.2f30fc45-42e2-c766-e063-6394a90a8d682025-02-28WarningsExact identifier
unii: OP1R32D61U
Fosinopril SodiumFOSINOPRIL SODIUMAurobindo Pharma Limitedaee04f17-8ee9-42f5-861f-b6ba17220ca42024-05-16Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 857183
rxcui: 857187
rxcui: 857169
unii: NW2RTH6T2N
Fosinopril Sodium and HydrochlorothiazideFOSINOPRIL SODIUM AND HYDROCHLOROTHIAZIDEAurobindo Pharma Limited35019655-9a30-4305-a262-936ad0e730712024-04-28Boxed warning, Warnings, Adverse reactionsExact identifier
unii: NW2RTH6T2N
Fosinopril SodiumFOSINOPRILBryant Ranch Prepackfc38f1bb-f175-4a81-8ed9-c8701efdea352023-11-27Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 857169
unii: NW2RTH6T2N
Fosinopril sodiumFOSINOPIRL SODIUMBryant Ranch Prepack3d521d4d-29f8-40d7-971b-0efb68dfbff22023-11-27Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA205670
rxcui: 857169
unii: NW2RTH6T2N
Fosinopril SodiumFOSINOPRILBryant Ranch Prepack6562a532-b502-4515-88df-591d71293b562023-10-19Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 857183
unii: NW2RTH6T2N
Fosinopril sodiumFOSINOPRIL SODIUMA-S Medication Solutions46e3e4e8-c611-4d4f-ad57-050b4c01fcd82023-09-25Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA205670
rxcui: 857187
unii: NW2RTH6T2N
Fosinopril sodiumFOSINOPRIL SODIUMBryant Ranch Prepackee78de8e-22f4-4c3b-a721-e9464d704eda2023-05-11Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA205670
ndc (package): 71335-9703-3
ndc (package): 71335-9703-1
ndc (package): 71335-9703-2
ndc (product): 71335-9703
ndc11 (package): 71335970301
rxcui: 857187
spl id: c526a852-6b47-4687-b543-f63e7aaf67e7
spl set id: ee78de8e-22f4-4c3b-a721-e9464d704eda
unii: NW2RTH6T2N
Fosinopril sodiumFOSINOPRIL SODIUMExelan Pharmaceuticals, Inc.e2ff3171-a17a-456a-9272-ca1682b01d192023-03-23Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 857183
rxcui: 857187
rxcui: 857169
unii: NW2RTH6T2N
Fosinopril SodiumFOSINOPRILA-S Medication Solutions880e5bf4-ced8-4765-a5c2-2361fd06ed9c2023-02-17Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 857187
rxcui: 857169
unii: NW2RTH6T2N
Fosinopril SodiumFOSINOPRILCipla USA Inc.736fe52f-69fb-48b2-b1c5-f065318785382023-01-20Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 857183
rxcui: 857187
rxcui: 857169
unii: NW2RTH6T2N
Fosinopril sodiumFOSINOPIRL SODIUMSolco Healthcare LLC0a66f606-5e6f-473d-8a1e-9ef316adb2e22021-10-25Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA205670
ndc (product): 43547-388
rxcui: 857183
rxcui: 857187
rxcui: 857169
spl id: e39b61db-42b8-4ddf-89d1-549c08d49e71
spl set id: 0a66f606-5e6f-473d-8a1e-9ef316adb2e2
unii: NW2RTH6T2N
Fosinopril Sodium and HydrochlorothiazideFOSINOPRIL SODIUM AND HYDROCHLOROTHIAZIDECIPLA USA INC.4e1ed7da-029e-48d6-a5e4-fc7ac11192fb2020-11-03Boxed warning, Warnings, Adverse reactionsExact identifier
unii: NW2RTH6T2N

Reported adverse events (FAERS/openFDA)#

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