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 4 of 7 · 123 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Ipratropium Bromide and Albuterol SulfateIPRATROPIUM BROMIDE AND ALBUTEROL SULFATENephron Pharmaceuticals Corporationae35ec1f-526a-49bf-8262-c50e40190d1f2025-04-08Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
Albuterol SulfateALBUTEROL SULFATEProficient Rx LPa6545fbe-b0a6-41ae-8bb6-91af38410f562025-04-01Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
ALBUTEROL SULFATEALBUTEROL SULFATEChartwell RX, LLC560df50c-e2c4-459f-9d89-bf7e6588949e2025-03-28Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
Albuterol SulfateALBUTEROL SULFATENephron Pharmaceuticals Corporationecc00500-58b8-491f-80df-dc6c89a08cae2025-03-21Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
AlbuterolALBUTEROLRising Pharma Holdings, Inc.40f3cdbc-c9ee-4a3c-8061-a44b9a1d035c2025-03-06Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
Albuterol SulfateALBUTEROL SULFATENuCare Pharmaceuticals,Inc.813d49be-3651-6759-e053-2991aa0a6a9f2025-02-06Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
Albuterol sulfateALBUTEROL SULFATELupin Pharmaceuticals, Inc.973b8686-c6ce-4280-85c4-c1e7ceab3c092025-01-23Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
Albuterol sulfateALBUTEROL SULFATEA-S Medication Solutions52e209ac-7156-4496-ba5a-42ee59d45deb2025-01-22Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
Albuterol SulfateALBUTEROL SULFATENuCare Pharmaceuticals,Inc.749992b4-69e0-0cc8-e053-2991aa0aeb252025-01-08Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
ALBUTEROL SULFATEALBUTEROL SULFATEHF Acquisition Co LLC, DBA HealthFirst9d4ef83f-8ca0-811e-e053-2995a90a6d0d2025-01-08Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
ALBUTEROL SULFATEALBUTEROL SULFATEPreferred Pharmaceuticals, Inc.4aafc2dd-744d-4726-828f-70355aee6f702025-01-03Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
Albuterol SulfateALBUTEROL SULFATEProficient Rx LP53eecdef-a7ff-4ca3-a313-d4b9c29c898d2025-01-01Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
Albuterol Sulfate HFAALBUTEROL SULFATEAdvanced Rx of Tennessee, LLC04c8a345-0a0d-5a01-e063-6294a90a40d22024-12-31Warnings, Adverse reactionsExact identifier
application number: NDA020983
rxcui: 2123076
unii: 021SEF3731
Albuterol SulfateALBUTEROL SULFATEAdvanced Rx Pharmacy of Tennessee, LLCf44b325d-0f74-552c-e053-2995a90ac1c92024-12-31Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
Albuterol Sulfate InhalationALBUTEROL SULFATEAmneal Pharmaceuticals NY LLC2e449282-ee58-4e36-b983-85c4e6f0864d2024-12-20Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
AlbuterolALBUTEROLZydus Lifesciences Limiteda4709eea-e4a2-46e2-850f-1e6afca018932024-11-25Exact identifier
unii: 021SEF3731
Albuterol SulfateALBUTEROL SULFATEIngenus Pharmaceuticals, LLCe14f5fd6-d01a-489d-9baa-61778b1352a82024-10-22Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
albuterol sulfateALBUTEROL SULFATEPadagis Israel Pharmaceuticals Ltd489201d2-9ed0-419b-81dc-a7f7f86b59ed2024-09-30Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
ALBUTEROL SULFATEALBUTEROL SULFATEBryant Ranch Prepack45e07bdd-78f9-4055-9de3-646e67de7eaf2024-08-15Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
ALBUTEROL SULFATEALBUTEROL SULFATELuoxin Aurovitas Pharma (Chengdu) Co., Ltd.1d6be2b8-c670-b783-e063-6294a90ae5032024-07-31Warnings, Adverse reactionsExact identifier
unii: 021SEF3731

Reported adverse events (FAERS/openFDA)#

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