Product Images Levalbuterol
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Product Label Images
The following 17 images provide visual information about the product associated with Levalbuterol NDC 0115-9930 by Amneal Pharmaceuticals Of New York Llc, 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 seems to be a label for a product called "FACE MASK RESERVOIR II". It provides no further information about the product or its purpose.*
This is a description of Levalbuterol Inhalation Solution, USP. Each 3 mL uni-dose vial contains 0.31 mg of levalbuterol provided as an aqueous solution containing sodium chloride, acetate sodium, and sulfuric acid to adjust the pH of the solution to 4.0. It provides quick relief from bronchospasms. The pack contains a "Patient Information Leaflet" and should be used only as directed by a physician. The unit-dose vials should remain stored in the protective pouch at all times. Once the pouch is opened, the vials should be used within two weeks. It is Rx only, and its mart is The Ritedose Corporation Distributed by Amneal Pharmaceuticals LLC.*
This is a product description of Levalbuterol Inhalation Solution, USP. Each 3 mL unit-dose vial contains 0.63 mg aqueous solution containing sodium. The solution is free from preservatives. This product is meant for inhalation use only, directed by a physician, and the recommended dosage must not be exceeded. The product should be stored at controlled room temperature and protected from light. The vials should remain in the protective pouch until use and once removed, they should be discarded after two weeks. The manufacturer is The Ritedose Corporation in South Carolina, and it is distributed by Amneal Pharmaceuticals LLC in Bridgewater, NJ. However, there is some text that is not readable or understandable.*
Levalbuterol Inhalation Solution, USP is a medication that comes in a unit-dose vial containing 1.25mg of the drug provided as hydrochloric salt in an aqueous solution along with sodium chloride, edetate disodium, and sulfuric acid to adjust the pH of the solution to 4.0. The package insert cautions that it should be used only as directed by a physician and not exceed the recommended dosage. It should be kept out of reach of children and stored in a protective pouch at controlled temperatures. The solution contains no preservatives.*
The text indicates that there is a shaded area that indicates the twist-off portion of a unit-dose vial.*
* 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.