FDA.reportPublic FDA data

NDC 68071-3064-06 - LISINOPRIL

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
68071-3064
Requested NDC
68071-3064-06
Package NDCs from labels
68071-3064-3, 68071-3064-5, 68071-3064-6, 68071-3064-9, 68071-3064-8, 68071-3064-2, 68071-3064-06
Manufacturer
NuCare Pharmaceuticals,Inc.
Effective date
2024-07-18
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
LISINOPRIL - NuCare Pharmaceuticals,Inc.NuCare Pharmaceuticals,Inc.2024-07-18HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
68071-3064-32021-02-11These highlights do not include all the information needed to use Lisinopril safely and effectively. See full prescribing information for Lisinopril LISINOPRIL tablets USP, for oral use Initial U.S. Approval: 1988
68071-3064-52021-02-11These highlights do not include all the information needed to use Lisinopril safely and effectively. See full prescribing information for Lisinopril LISINOPRIL tablets USP, for oral use Initial U.S. Approval: 1988
68071-3064-62021-02-11These highlights do not include all the information needed to use Lisinopril safely and effectively. See full prescribing information for Lisinopril LISINOPRIL tablets USP, for oral use Initial U.S. Approval: 1988
68071-3064-82021-02-11These highlights do not include all the information needed to use Lisinopril safely and effectively. See full prescribing information for Lisinopril LISINOPRIL tablets USP, for oral use Initial U.S. Approval: 1988
68071-3064-92021-02-11These highlights do not include all the information needed to use Lisinopril safely and effectively. See full prescribing information for Lisinopril LISINOPRIL tablets USP, for oral use Initial U.S. Approval: 1988
68071-3064-32021-01-29These highlights do not include all the information needed to use Lisinopril safely and effectively. See full prescribing information for Lisinopril LISINOPRIL tablets USP, for oral use Initial U.S. Approval: 1988
68071-3064-52021-01-29These highlights do not include all the information needed to use Lisinopril safely and effectively. See full prescribing information for Lisinopril LISINOPRIL tablets USP, for oral use Initial U.S. Approval: 1988
68071-3064-62021-01-29These highlights do not include all the information needed to use Lisinopril safely and effectively. See full prescribing information for Lisinopril LISINOPRIL tablets USP, for oral use Initial U.S. Approval: 1988
68071-3064-82021-01-29These highlights do not include all the information needed to use Lisinopril safely and effectively. See full prescribing information for Lisinopril LISINOPRIL tablets USP, for oral use Initial U.S. Approval: 1988
68071-3064-92021-01-29These highlights do not include all the information needed to use Lisinopril safely and effectively. See full prescribing information for Lisinopril LISINOPRIL tablets USP, for oral use Initial U.S. Approval: 1988

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68071-3064-2LISINOPRIL120 in 1 BOTTLETABLET1206
68071-3064-3LISINOPRIL30 in 1 BOTTLETABLET306
68071-3064-5LISINOPRIL45 in 1 BOTTLETABLET456
68071-3064-6LISINOPRIL60 in 1 BOTTLETABLET606
68071-3064-8LISINOPRIL180 in 1 BOTTLETABLET1806
68071-3064-9LISINOPRIL90 in 1 BOTTLETABLET906

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68071-3064LISINOPRIL TABLET [NUCARE PHARMACEUTICALS,INC.]6Current NDC, Legacy NDC, 6 package rows20240720_6314e49c-8715-2f01-e053-2a91aa0ab2a5.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 3 of 41 · 814 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
LISINOPRILLISINOPRILREMEDYREPACK INC.42f49299-7ae5-4d30-86eb-66b739c0e95d2026-07-14Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 311353
unii: E7199S1YWR
Jacksons Cell Salts SILICA 12X 12SILICEAZettl Health Inc.5647dafc-1fff-6a25-e063-6294a90a8b4f2026-07-10Exact identifier
unii: ETJ7Z6XBU4
LISINOPRILLISINOPRILREMEDYREPACK INC.12d6fe7e-b5a2-4d49-9a06-a6150234d0612026-07-08Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA076164
rxcui: 197884
unii: E7199S1YWR
LISINOPRILLISINOPRILCoupler LLC560513ef-4d2c-8ca0-e063-6394a90a674a2026-07-07Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA076164
rxcui: 311354
unii: E7199S1YWR
LisinoprilLISINOPRILA-S Medication Solutions88b5a2c0-6ad2-48e7-9ffe-715d9159f3892026-07-06Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 311354
unii: E7199S1YWR
LisinoprilLISINOPRILA-S Medication Solutions34953f77-bae1-41fe-af11-3ea0b3ceaa112026-07-06Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 314077
rxcui: 197884
rxcui: 314076
rxcui: 311353
rxcui: 311354
unii: E7199S1YWR
LisinoprilLISINOPRILREMEDYREPACK INC.3451292b-7867-4dc2-afaa-da66b40160172026-07-03Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 314077
unii: E7199S1YWR
LisinoprilLISINOPRILREMEDYREPACK INC.d32923fe-a323-43c6-af46-bcba7274b0bf2026-07-03Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 311353
unii: E7199S1YWR
The Cell Salt Co. Daily Blend 12 in 1CALC FLUOR, CALC PHOS, CALC SULPH, FERRUM PHOS, KALI MUR, KALI PHOS, KALI SULPH, MAG PHOS, NAT MUR, NAT PHOS, NAT SULPH, SILICEAThe Cell Salt Company LLC55826f59-acf4-7370-e063-6394a90afed72026-07-01WarningsExact identifier
unii: ETJ7Z6XBU4
LISINOPRILLISINOPRILREMEDYREPACK INC.e17bcc2e-f5ed-4846-95d3-a5479c7fee8d2026-07-01Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA076164
rxcui: 314077
unii: E7199S1YWR
Lisinopril and HydrochlorothiazideLISINOPRIL AND HYDROCHLOROTHIAZIDE TABLETSSt. Mary's Medical Park Pharmacye1aa9682-b1ad-4a22-e053-2a95a90a0e2f2026-06-30Boxed warning, Warnings, Adverse reactionsExact identifier
unii: E7199S1YWR
Bambusa StannumBAMBUSA STANNUMUriel Pharmacy Inc.a0d4d0ac-e2d2-4381-8f93-e417195218592026-06-30WarningsExact identifier
unii: ETJ7Z6XBU4
LISINOPRILLISINOPRILSt. Mary's Medical Park Pharmacy5f4c1a62-fb84-8cdc-e053-2a91aa0a671a2026-06-26Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA076164
rxcui: 314077
unii: E7199S1YWR
Lisinopril and HydrochlorothiazideLISINOPRIL AND HYDROCHLOROTHIAZIDEREMEDYREPACK INC.3857ac53-0435-4d68-8066-c222914148892026-06-25Boxed warning, Warnings, Adverse reactionsExact identifier
unii: E7199S1YWR
LisinoprilLISINOPRILUnit Dose Solutions, Inc.551665a0-9a92-55df-e063-6394a90a1e2e2026-06-25Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 314076
unii: E7199S1YWR
LisinoprilLISINOPRILUnit Dose Solutions, Inc.55189717-f5db-9c63-e063-6294a90a6bc92026-06-25Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 314077
unii: E7199S1YWR
LisinoprilLISINOPRILUnit Dose Solutions, Inc.55191baa-f812-2e71-e063-6294a90a8edf2026-06-25Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 311354
unii: E7199S1YWR
Lisinopril and HydrochlorothiazideLISINOPRIL AND HYDROCHLOROTHIAZIDEREMEDYREPACK INC.868b1442-c412-4ee8-9798-f2408cd2249a2026-06-24Boxed warning, Warnings, Adverse reactionsExact identifier
unii: E7199S1YWR
Lisinopril and HydrochlorothiazideLISINOPRIL AND HYDROCHLOROTHIAZIDEREMEDYREPACK INC.408e797a-2cf3-4ee6-9f9b-179a8cf3d7992026-06-23Boxed warning, Warnings, Adverse reactionsExact identifier
unii: E7199S1YWR
H-Scars FormulaCALENDULA OFFICINALLIS, SILICEAHealing Natural Oils LLC8433ff00-d815-45e0-b0ec-1448668dd8f82026-06-16WarningsExact identifier
unii: ETJ7Z6XBU4

Reported adverse events (FAERS/openFDA)#

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