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Arformoterol Tartrate Solution
Product Images NDC 70748-175
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Product Visual Gallery
This gallery contains 11 technical images submitted to the FDA as part of the official labeling for Arformoterol Tartrate (NDC 70748-175). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Lupin Pharmaceuticals, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Product Images & Figures Index
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This text appears to be a table with numerical values indicating mean change from basal FEV at various hours postdose for a placebo group and a group treated with 15 mcg Arformoterol Tartrate Inhalation Solution BID. The baseline FEV1 for the placebo group is 1.20 (L) and for the treated group is 1.15 (L). No further context or information is provided.*
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This is a description of a medication called Arformoterol Tartrate that comes in a unit-dose vial. It is an inhalation solution with a potency expressed as arformoterol. The vial contains 15 mg of arformoterol squalene, which equates to 22 mcg of arformoterol. The solution is packed in a pouch and is meant to be opened just before use. The vial should be kept out of reach of children and protected from excessive heat and light. The unopened pouches with unit-dose vials can be stored in a refrigerator at 36°F to 46°F or at a temperature of 20°C to 25°C for up to ten weeks. The medication label includes the lot number and manufacturing details. The product should be used before the expiration date.*
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* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
