Blisovi 24 Fe Kit
Product Images NDC 68180-864

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Blisovi 24 Fe (NDC 68180-864). 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.

FDA Label Image

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This appears to be a list of studies related to women's contraceptive use and their health, along with a column labeled "Effect Estimate (OR/RR)" which could possibly refer to odds ratios or relative risks. The list is not well-formatted and contains some errors, such as missing spaces and misaligned parentheses, making it difficult to decipher the exact details and conclusions of the studies.*

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This is a medication package for Blisovi 24 Fe, a combination of norethindrone acetate and ethinyl estradiol tablets, with added ferrous fumarate tablets. The package has information about dosage, manufacturer and lot number. It also includes an image of the forming foil/PVC side and lidding foil side, and a suggested monthly self-breast exam.*

FDA Label Image

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Blisovi 24 Fe is a prescription medicine that contains norethindrone acetate and ethinyl estradiol tablets USP and ferrous fumarate tablets. It is used as a form of contraceptive therapy and does not protect against HIV infection or pregnancy. The NDC number is 68150-864.71. The text also includes some other numbers and words that are not clear.*

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This appears to be a prescription for Blisovi 24 Fe, a type of birth control pill, in different dosages. It is not clear what the dosages are as the text is not readable.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.