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 3 of 7 · 123 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
AlbuterolALBUTEROL SULFATECipla USA Inc.fd0389e0-3713-42e0-8ef2-3bb97676fded2026-01-04Warnings, Adverse reactionsExact identifier
rxcui: 2123076
unii: 021SEF3731
ALBUTEROL SULFATEALBUTEROL SULFATEChartwell Governmental & Specialty RX, LLC.dd47559a-84f6-42a5-a00e-48754505418e2025-12-17Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
Albuterol SulfateALBUTEROL SULFATESandoz Incf8a2c4b7-a162-48ab-90b0-350e4da25c662025-12-16Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
IPRATROPIUM BROMIDE AND ALBUTEROL SULFATEIPRATROPIUM BROMIDE AND ALBUTEROL SULFATERitedose Pharmaceuticals, LLCe0dee492-8bf9-4360-be9b-9d6ee1ecb2562025-12-10Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
Ipratropium Bromide and Albuterol SulfateIPRATROPIUM BROMIDE AND ALBUTEROL SULFATEChartwell RX, LLCb444478a-10ce-484f-9039-6383dfb8161e2025-12-02Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
Combivent RespimatIPRATROPIUM BROMIDE AND ALBUTEROLBoehringer Ingelheim Pharmaceuticals, Inc.9832312e-0310-4ab6-8501-afa976fc7eb22025-12-01Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
ALBUTEROL SULFATEALBUTEROL SULFATEBryant Ranch Prepack378461f2-7271-44a3-9da3-b39970b65d3a2025-11-10Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
Albuterol SulfateALBUTEROL SULFATENephron Pharmaceuticals Corporation574824f3-51cc-4b94-9c10-e3204d8b19f82025-11-07Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
Albuterol SulfateALBUTEROL SULFATEASCLEMED USA INC.8ea40065-4f59-434f-9ea1-7ef006fde66e2025-11-07Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
Albuterol SulfateALBUTEROL SULFATEAsclemed USA, Inc.056e145b-87aa-4009-a7ab-2ac0bd086eb02025-11-06Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
Albuterol SulfateALBUTEROL SULFATENuCare Pharmaceuticals, Inc.2c3f975c-dbd8-0362-e063-6394a90a16dd2025-10-21Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
Albuterol SulfateALBUTEROL SULFATENuCare Pharmaceuticals,Inc.4120061a-dbae-8918-e063-6394a90afbf22025-10-14Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
Albuterol SulfateALBUTEROL SULFATEPreferred Pharmaceuticals, Inc.081b7bbb-6692-4512-b135-863b73bf30a52025-10-13Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
AIRSUPRAALBUTEROL SULFATE AND BUDESONIDEAstraZeneca Pharmaceuticals LPe60aa9f9-5139-44df-b886-ebddc3c7eb132025-09-18Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
Albuterol Sulate HFAALBUTEROL SULFATENuCare Pharmaceuticals,Inc.825975b1-a4a9-78ca-e053-2a91aa0a39482025-09-02Warnings, Adverse reactionsExact identifier
application number: NDA020983
rxcui: 2123076
unii: 021SEF3731
ALBUTEROL SULFATEALBUTEROL SULFATEQUAGEN PHARMACEUTICALS LLC99a490cc-e41d-436b-9cf3-8facb7ac714f2025-07-03Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
Albuterol sulfateALBUTEROL SULFATEPreferred Pharmaceuticals, Inc.99782bc8-56d9-41f8-935e-0d0de27f0c342025-05-19Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
Albuterol SulfateALBUTEROL SULFATEPreferred Pharmaceuticals Inc.1c72fd84-7dbc-45d0-ab88-fb4221ce369f2025-05-16Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
Albuterol sulfateALBUTEROL SULFATEAsclemed USA, Inc.264e2145-c7d4-4f4f-aa5b-9fe48a7c5b472025-05-07Warnings, Adverse reactionsExact identifier
unii: 021SEF3731
AlbuterolALBUTEROLBryant Ranch Prepack601a18ed-d66e-498f-a804-f1a3330827d42025-04-21Warnings, Adverse reactionsExact identifier
unii: 021SEF3731

Reported adverse events (FAERS/openFDA)#

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