Norethindrone
Product Images NDC 0378-7272

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Norethindrone (NDC 0378-7272). 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

Structure (Dcc81f04 856f 46a8 998a 288a394d0092 01)

Chemical structure of norethindrone showing its steroid backbone with a hydroxyl group, a methyl group, a ketone group, and an ethynyl group attached to the ring system.*

FDA Label Image

Image 01

Packaging label for Norethindrone Tablets, USP 0.35 mg by Mylan Pharmaceuticals Inc. The carton states the product is an oral contraceptive in a 28-day regimen, with 3 pouches each containing 28 tablets. The label includes storage instructions and directs to the package insert for full prescribing information. The label also shows the NDC 0378-7272-53 and contains manufacturer information.*

FDA Label Image

Image 02

Norethindrone Tablets, USP, 0.35 mg blister card from Mylan Pharmaceuticals Inc., containing 28 tablets. The label includes instructions for Day-1 starters and Sunday starters with a weekly layout showing days from Sunday to Saturday, guiding pill intake from left to right each week. Storage information specifies 20° to 25°C (68° to 77°F).*

FDA Label Image

Image 03

An instructional diagram for Norethindrone medication showing day label strips for a weekly pill schedule. It includes rows of day abbreviations (Mon-Sun) for aligning the strip with the blister pack days. Below, instructions guide on selecting the correct day label strip based on the first day of the menstrual period, to ensure correct pill intake.*

* 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.