Product Images Albuterol Sulfate
View Photos of Packaging, Labels & Appearance
Product Label Images
The following 18 images provide visual information about the product associated with Albuterol Sulfate NDC 70518-3541 by Remedyrepack Inc., such as packaging, labeling, and the appearance of the drug itself. This resource could be helpful for medical professionals, pharmacists, and patients seeking to verify medication information and ensure they have the correct product.
The text is a table or a chart showing the percentage change in FEV over time (in hours) for three different types of inhalers: Albuterol Sulfate Inhalation Aerosol, Matched Placebo HFA Inhalation Aerosol, and Marketed HFA-134a Albuterol Inhaler. The sample sizes for each type of inhaler are also specified.*
This appears to be a graph showing the change in FEV (Forced Expiratory Volume) over time in hours for three groups of inhalers: Albuterol Sulfate Inhalation Aerosol, a matched Placebo HFA Inhalation Aerosol, and a marketed HFA-134a Albuterol Inhaler. The graph shows that the Albuterol Sulfate Inhalation Aerosol had the highest increase in FEV, followed by the marketed HFA-134a Albuterol Inhaler, and the matched placebo had the smallest change in FEV.*
This is a description of a metal canister that comes with a plastic actuator, a label, and a mouthpiece. It does not provide any further information about the products or their uses.*
This text provides instructions on how to clean a mouthpiece by washing it under warm running water.*
This text suggests the use of a mouthpiece that needs to be kept dry, preferably overnight. It could refer to a dental appliance or musical instrument accessory.*
Albuterol Sulfate is an inhalation aerosol with 200 metered inhalations, and 90 mcg per actuation. It is for oral inhalation only when used with the enclosed actuator. The medication has a quantity of 859g and should be stored at 20-25°C (88-77°F) with permission to store at 15-30°C (59-86°F) for excursions (See USP). It is prescribed only by physicians and if the dosage does not provide relief, users should contact their physician. The expiration date and lot number are not available, and it was repackaged by RemedyRepack Inc. in Indiana. The source NDC is 68180-0963-01, and it is manufactured by Lupin Pharma in Baltimore, MD. Users should keep the medication out of the reach of children.*
* The product label images have been analyzed using a combination of traditional computing and machine learning techniques. It should be noted that the descriptions provided may not be entirely accurate as they are experimental in nature. Use the information in this page at your own discretion and risk.