FDA.reportPublic FDA data

NDC 68071-1890-06 - VENTOLIN HFA

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
68071-1890
Requested NDC
68071-1890-06
Package NDCs from labels
68071-1890-6, 68071-1890-06
Manufacturer
NuCare Pharmaceuticals,Inc.
Effective date
2024-07-16
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
VENTOLIN HFA - NuCare Pharmaceuticals,Inc.NuCare Pharmaceuticals,Inc.2024-07-16HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68071-1890-62023-02-10C16284748780-1f386c64a-002f-0266-e053-dadaa90a7c1aThese highlights do not include all the information needed to use VENTOLIN HFA safely and effectively. See full prescribing information for VENTOLIN HFA. VENTOLIN HFA (albuterol sulfate) Inhalation Aerosol FOR ORAL INHALATION Initial U.S. Approval: 1981
68071-1890-62023-01-30C16284748780-1f386c64a-002f-0266-e053-dadaa90a7c1aThese highlights do not include all the information needed to use VENTOLIN HFA safely and effectively. See full prescribing information for VENTOLIN HFA. VENTOLIN HFA (albuterol sulfate) Inhalation Aerosol FOR ORAL INHALATION Initial U.S. Approval: 1981

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68071-1890-6VENTOLINHFA60 in 1 BOXAEROSOL, METERED607

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68071-1890VENTOLIN HFA (ALBUTEROL SULFATE) AEROSOL, METERED [NUCARE PHARMACEUTICALS,INC.]7Current NDC, Legacy NDC, 1 package rows20240717_7043bc12-8a58-8ff8-e053-2a91aa0ab627.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 2 of 7 · 121 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Albuterol SulfateALBUTEROL SULFATESportpharm LLCe31d8d13-ac19-4738-97d4-d7790ce2e8e32026-04-24Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
Albuterol sulfateALBUTEROL SULFATESportpharm LLC32d954ee-9790-4beb-95db-72dbf8efa6392026-04-24Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
Albuterol SulfateALBUTEROL SULFATECardinal Health 107, LLCd2132c1c-0f90-4c6f-afc0-f3814b6a7e5c2026-04-20Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
albuterol sulfateALBUTEROL SULFATEGolden State Medical Supply, Inc.a22af54a-c010-ab8b-e053-2a95a90a88622026-04-15Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
AlbuterolALBUTEROLAmneal Pharmaceuticals NY LLC230d66fc-f62c-42a6-adb3-0a0f879c8ad42026-04-14Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
Albuterol sulfateALBUTEROL SULFATEREMEDYREPACK INC.0cfb6c5d-eac2-4a1c-8a0f-6b00e819adda2026-04-13Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
Ipratropium Bromide and Albuterol SulfateIPRATROPIUM BROMIDE AND ALBUTEROL SULFATESun Pharmaceutical Industries, Inc.38f9a201-3954-4370-8e71-7ec2df88a1ff2026-04-09Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
Albuterol SulfateALBUTEROL SULFATESun Pharmaceutical Industries, Inc.bb538b7d-e390-419a-9404-a57c1db4a4472026-04-09Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
Albuterol SulfateALBUTEROL SULFATECardinal Health 107, LLC6ec88f64-66a2-4ca9-9913-c192fc33f88b2026-04-08Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
Albuterol SulfateALBUTEROL SULFATENephron Pharmaceuticals Corporation285a656c-f77f-4e77-b0a8-a0e9c901803f2026-04-06Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
albuterol sulfateALBUTEROL SULFATESun Pharmaceutical Industries, Inc.87b8cd3c-2849-4b50-b63e-9ea379165c072026-03-16Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
AlbuterolALBUTEROLMylan Pharmaceuticals Inc.9e6e982b-7dfe-45b8-aa76-754e8d2a8ef62026-03-15Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
Albuterol SulfateALBUTEROL SULFATEPreferred Pharmaceuticals Inc.c90e80b2-882e-4c0c-bfac-d67eb1da724d2026-02-16Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
Albuterol SulfateALBUTEROL SULFATEMylan Pharmaceuticals Inc.5329614f-ae0b-4854-bb6f-ea0b7dae87c02026-02-10Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
Albuterol Sulate HFAALBUTEROL SULFATEREMEDYREPACK INC.77d34a3c-ccc6-420a-ad31-a1af55f7de762026-01-30Warnings, Adverse reactionsExact identifier
application number: NDA020983
rxcui: 2123076
unii: 021SEF3731
IPRATROPIUM BROMIDE AND ALBUTEROL SULFATEIPRATROPIUM BROMIDE AND ALBUTEROL SULFATEGolden State Medical Supply, Inc.2ebc820b-a423-46ef-8eba-9fbc93daff442026-01-28Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
Albuterol SulfateALBUTEROL SULFATEPreferred Pharmaceuticals Inc.1f0bf143-66d4-4a39-b2d1-a5c460ffdcf92026-01-22Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
VENTOLIN HFAALBUTEROL SULFATEREMEDYREPACK INC.2ed73618-be3a-4331-9509-6401258f791f2026-01-19Warnings, Adverse reactionsExact identifier
application number: NDA020983
rxcui: 801092
rxcui: 801095
unii: 021SEF3731
Albuterol SulfateALBUTEROL SULFATEPreferred Pharmaceuticals Inc.5de6a189-a8b7-4b33-b162-add6b6e4b2752026-01-16Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
Albuterol SulfateALBUTEROL SULFATEPreferred Pharmaceuticals Inc.d6acb5a7-555a-463a-ae65-2911d6789b422026-01-14Warnings, Adverse reactionsExact identifier
unii: 021SEF3731

Reported adverse events (FAERS/openFDA)#

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