FDA.reportPublic FDA data

NDC 70518-1237-00 - 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
70518-1237
Requested NDC
70518-1237-00
Package NDCs from labels
70518-1237-0, 70518-1237-00
Manufacturer
REMEDYREPACK INC.
Effective date
2026-01-19
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
VENTOLIN HFA - REMEDYREPACK INC.REMEDYREPACK INC.2026-01-19HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70518-1237-0VENTOLINHFA60 in 1 INHALERAEROSOL, METERED6013
70518-1237-0VENTOLINHFA1 in 1 CARTONAEROSOL, METERED113

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70518-1237VENTOLIN HFA (ALBUTEROL SULFATE) AEROSOL, METERED [REMEDYREPACK INC.]12Current NDC, Legacy NDC, 2 package rows20250509_2ed73618-be3a-4331-9509-6401258f791f.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 5 of 7 · 123 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ALBUTEROL SULFATEALBUTEROL SULFATEAurobindo Pharma Limited78e6bee2-7113-46cf-8c97-dc61b0f7b94f2024-07-31Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
Albuterol SulfateALBUTEROL SULFATEAmerican Health Packagingb0f73459-baeb-42a7-be48-2c3647d9b2052024-07-30Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
Albuterol sulfateALBUTEROL SULFATENuCare Pharmaceuticals,Inc.b478d9e9-9704-6af2-e053-2995a90aafd42024-07-17Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
VENTOLIN HFAALBUTEROL SULFATENuCare Pharmaceuticals,Inc.7043bc12-8a58-8ff8-e053-2a91aa0ab6272024-07-16Warnings, Adverse reactionsExact identifier
application number: NDA020983
rxcui: 801092
rxcui: 801095
unii: 021SEF3731
VENTOLIN HFAALBUTEROL SULFATENuCare Pharmaceuticals,Inc.54d90668-5237-4330-e054-00144ff88e882024-07-15Warnings, Adverse reactionsExact identifier
application number: NDA020983
rxcui: 859088
rxcui: 2123076
unii: 021SEF3731
Albuterol Sulfate HFAALBUTEROL SULFATENuCare Pharmaceuticals,Inc.8c278b6f-d32b-b750-e053-2995a90ad7e92024-06-18Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
IPRATROPIUM BROMIDE AND ALBUTEROL SULFATEIPRATROPIUM BROMIDE AND ALBUTEROL SULFATEA-S Medication Solutionse452afc2-dc33-4be7-949e-143b2e5f530c2024-06-10Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
IPRATROPIUM BROMIDE AND ALBUTEROL SULFATEIPRATROPIUM BROMIDE AND ALBUTEROL SULFATEAmerican Health Packagingc04c6ec8-1401-424d-8126-63080e36c4b92024-06-03Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
VENTOLIN HFAALBUTEROL SULFATEA-S Medication Solutionsaa6d5c00-46a5-4f93-95e4-09319abfe71e2024-05-07Warnings, Adverse reactionsExact identifier
application number: NDA020983
rxcui: 801092
rxcui: 801095
unii: 021SEF3731
Albuterol SulfateALBUTEROL SULFATEA-S Medication Solutions19867b61-77a2-46f1-97c7-7fadfec5882b2024-05-07Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
VENTOLIN HFAALBUTEROL SULFATEA-S Medication Solutionsaff836e4-34f2-4ab9-bbf8-0c41ac848cb02024-05-07Warnings, Adverse reactionsExact identifier
application number: NDA020983
rxcui: 859088
rxcui: 2123076
unii: 021SEF3731
Albuterol Sulfate HFAALBUTEROL SULFATEPrasco Laboratoriesb25d9d6b-eb4c-452e-89ef-10e611deebd62024-04-30Warnings, Adverse reactionsExact identifier
application number: NDA020983
rxcui: 2123076
unii: 021SEF3731
VENTOLIN HFAALBUTEROL SULFATEGlaxoSmithKline LLCd92c5d6b-ff10-4087-36a2-1cfc464cb9672024-04-26Warnings, Adverse reactionsExact identifier
application number: NDA020983
ndc (product): 0173-0682
rxcui: 859088
rxcui: 801092
rxcui: 801095
rxcui: 2123076
spl id: 08d3613c-b059-4e06-b42c-591a129f1649
spl set id: d92c5d6b-ff10-4087-36a2-1cfc464cb967
unii: 021SEF3731
ALBUTEROL SULFATEALBUTEROL SULFATEHF Acquisition Co LLC, DBA HealthFirst767a1504-1e04-1e06-e053-2a91aa0aa4b62024-02-22Warnings, Adverse reactionsExact identifier
application number: NDA020983
rxcui: 801092
unii: 021SEF3731
Albuterol SulfateALBUTEROL SULFATEChartwell RX, LLC.7f261a9b-65d9-408a-8609-c1b3809b8b4b2024-02-21Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
Albuterol SulfateALBUTEROL SULFATEChartwell RX, LLC4e48ccbe-3ec0-4bf2-be28-83eb9baa63d62024-02-21Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
Albuterol SulfateALBUTEROL SULFATEChartwell RX, LLC922bf33b-4d55-4c35-9f68-72efbb17c14f2024-02-21Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
ALBUTEROL SULFATEALBUTEROL SULFATEA-S Medication Solutions7ad17b39-d2de-4108-abbf-cedd650c8edd2024-02-18Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
Ipratropium Bromide and Albuterol SulfateIPRATROPIUM BROMIDE AND ALBUTEROL SULFATECipla USA Inc.89d59bd9-c826-413c-8ed9-a1521a0c7cc52024-01-11Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
Ipratropium Bromide and Albuterol SulfateIPRATROPIUM BROMIDE AND ALBUTEROL SULFATEProficient Rx LPa1d9d346-91a5-4f5a-82ed-4ebeaf350a062024-01-01Warnings, Adverse reactionsExact identifier
unii: 021SEF3731

Reported adverse events (FAERS/openFDA)#

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