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
Label	Manufacturer	Effective date	Type
VENTOLIN HFA - REMEDYREPACK INC.	REMEDYREPACK INC.	2026-01-19	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70518-1237-0	VENTOLINHFA	60 in 1 INHALER	AEROSOL, METERED	60		13
70518-1237-0	VENTOLINHFA	1 in 1 CARTON	AEROSOL, METERED	1		13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70518-1237	VENTOLIN HFA (ALBUTEROL SULFATE) AEROSOL, METERED [REMEDYREPACK INC.]	12	Current NDC, Legacy NDC, 2 package rows	20250509_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 7 of 7 · 123 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
ALBUTEROL SULFATE	ALBUTEROL SULFATE	Exelan Pharmaceuticals, Inc.	29e35e54-dbd6-4426-993f-893d7a4d69be	2022-02-10	Warnings, Adverse reactions	Exact identifier unii: 021SEF3731
Albuterol Sulfate	ALBUTEROL SULFATE	Asclemed USA, Inc.	8153d82c-b5c5-4aa2-bce5-b69cf2d23f5d	2020-10-16	Warnings, Adverse reactions	Exact identifier unii: 021SEF3731
Ipratropium Bromide and Albuterol Sulfate	IPRATROPIUM BROMIDE AND ALBUTEROL SULFATE	Mylan Pharmaceuticals Inc.	23c05e9a-9df5-4978-8831-cf562aa4ba92	2018-12-12	Warnings, Adverse reactions	Exact identifier unii: 021SEF3731

Reported adverse events (FAERS/openFDA)#

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