Norgestimate And Ethinyl Estradiol Kit
Product Images NDC 68180-840

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Norgestimate And Ethinyl Estradiol (NDC 68180-840). 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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An instructional calendar diagram for Norgestimate and Ethinyl Estradiol showing a 28-day pill regimen divided by weeks and days from Sunday to Saturday. It includes arrows indicating the order of pill intake and a note to place a day label strip for periods starting on days other than Sunday. The diagram also reminds users to perform a monthly self-breast exam.*
FDA Label Image

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A forest plot chart titled 'Risk of Breast Cancer with Combined Oral Contraceptive Use,' showing effect estimates (OR/RR) and confidence intervals for various studies. The horizontal axis ranges from -1.5 to 2, with study names and years listed on the left, and numerical effect estimates with confidence intervals on the right. Black dots and horizontal lines represent point estimates and confidence intervals for each study's findings.*
FDA Label Image

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Chemical structure diagram showing the molecular formulas of the active ingredients Norgestimate and Ethinyl Estradiol, with labeled functional groups on each steroid-based structure.*
FDA Label Image

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A vertical chart illustrating pregnancy rates by contraceptive method, with 'Fewer Pregnancies' at the top and 'More Pregnancies' at the bottom. It categorizes contraceptive methods from most to least effective, including implants, injections, intrauterine devices, sterilization, birth control pills, skin patch, vaginal ring, condoms, diaphragm, no sex during fertile days, spermicide, withdrawal, and no birth control.*
FDA Label Image

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An illustrated weekly calendar guide for a 28-day pill pack for Norgestimate and Ethinyl Estradiol by Lupin Pharmaceuticals, Inc. It shows circles arranged in a four-week horizontal grid labeled Sunday through Saturday with arrows indicating the pill-taking sequence. The top of the chart instructs users to align the day label strip with the start day of their period, and there is a reminder for a monthly self breast exam.*
FDA Label Image

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Lidding foil and forming foil/PVC side of a blister pack for Norgestimate and Ethinyl Estradiol Tablets USP 0.25 mg/0.035 mg from Lupin Pharmaceuticals, Inc. The lidding foil side displays the product name, dosage, storage instructions, distributor, manufacturer, lot and expiration fields, and NDC 68180-840. The forming foil/PVC side shows a 28-day pill schedule labeled by weeks and days with circular slots for tablets and a monthly self breast exam reminder.*
FDA Label Image

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Packaging label for Norgestimate and Ethinyl Estradiol Tablets USP, containing 0.25 mg/0.035 mg strength. The label states it is an oral contraceptive with 1 blister of 28 tablets, distributed and manufactured by Lupin Pharmaceuticals, Inc. The label includes usage notes, barcodes, and lot/expiration placeholders, on a pink and orange gradient background.*
FDA Label Image

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Packaging label for Norgestimate and Ethinyl Estradiol Tablets USP 0.25 mg/0.035 mg distributed by Lupin Pharmaceuticals, Inc. The label shows product name, strength, dosage form, NDC 68180-840-73, and mentions three blisters of 28 tablets each. It includes usage warnings, manufacturer Lupin Limited in India, barcodes, and a pink-yellow gradient background with Lupin logo.*

* 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.