Norethindrone Acetate And Ethinyl Estradiol Tablet
Product Images NDC 0378-7274

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Norethindrone Acetate And Ethinyl Estradiol (NDC 0378-7274). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mylan 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

Structures (17eb0f03 1827 4bd3 A633 390500bdf250 01)

Norethindrone Acetate is a medication used as a form of birth control, and for treating menstrual disorders, endometriosis, and other conditions related to the uterus.*

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Graph (17eb0f03 1827 4bd3 A633 390500bdf250 02)

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Blister With Instructions (17eb0f03 1827 4bd3 A633 390500bdf250 03)

This is a set of instructions for women starting their birth control pill pack, providing guidance for both Sunday and Day-1 starters. Day-1 starters should place the label strip with the first day of their period on the box, and take the pills in the direction from left to right each week. The box contains Norethindrone Acetate and Ethinyl Estradiol Tablets USP, 1.5 mg/003 mg, which should be stored at controlled room temperature. NDC 0378-7274-85 is the Rx-only product identifier.*

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Day Sticker Label (17eb0f03 1827 4bd3 A633 390500bdf250 04)

This appears to be a set of instructions related to a menstrual cycle tracking tool. The tool includes day label strips that correspond to the days of the week, starting with Sunday. The user is instructed to choose a strip that matches the start day of their period and place it over the preprinted days of the week on the tool. The instructions note that if the period starts on a Sunday, this step can be skipped.*

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Blister With Instructions (17eb0f03 1827 4bd3 A633 390500bdf250 05)

This document provides instructions for both Sunday starters and Day-1 starters of Norethindrone Acetate and Ethinyl Estradiol Tablets USP, 1.5 mg/003 mg. If the period starts on a day other than Sunday, the user should place the day label strip starting with the first day of the period. The pills should be taken from left to right each week, as indicated on the document. The pharmaceutical should be stored at room temperature.*

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Day Sticker Label (17eb0f03 1827 4bd3 A633 390500bdf250 06)

This text appears to be instructions for using a period tracking product, and provides guidance on how to choose and place a label strip that corresponds to the user's menstrual period cycle. It also indicates that if the first day of the user's period is a Sunday, a step can be skipped.*

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3s Carton (Image 01)

This is an -scanned text of a medication called Norethindrone Acetate and Ethinyl Estradiol Tablets. It is used as an oral contraceptive and is intended to prevent pregnancy. It is not meant to protect against HIV and other sexually transmitted diseases. Each blister pack contains 21 blue tablets with a dosage of 1.5mg Norethindrone Acetate and 0.03 mg Ethinyl Estradiol. The patient instructions enclosed in the package are important. The dosage should be taken as prescribed, and the medication should be stored at room temperature. It is crucial to keep it away from children.*

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Image 02

This text provides a list of studies and their effect estimates comparing the use of combined oral contraceptives (COC) to non-use or current use for various health outcomes. The studies include NICHD Women's Care Study, French E3N cohort Study, Shanghal Women's Health Study, The Nurses’ Health Study II, and Oxford Family Planning Study. The effect estimates are in the form of odds ratios (OR), relative risks (RR), and hazard ratios (HR). However, the specific health outcomes are not mentioned in the text.*

* 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.