Norethindrone
Product Images NDC 76413-118

3 FDA label images from Central Texas Community Health Centers · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Norethindrone (NDC 76413-118). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Central Texas Community Health Centers, 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

FDA Label Image

Structure (Nor Qd1 Figure 01)

Structure (Nor Qd1 Figure 01)
Chemical structure of norethindrone, showing its molecular rings and functional groups. The diagram includes hydroxyl (OH), methyl (CH3), ketone (O), and an alkyne (C≡CH) moiety characteristic of the steroidal backbone.*
FDA Label Image

Figure 1 (Nor Qd1 Figure 02)

Figure 1 (Nor Qd1 Figure 02)
A pharmacokinetic graph depicting the concentration (Cp) in pg/mL of Norethindrone over time in hours after oral administration of a 0.35 mg dose. The graph shows a rapid initial decline in concentration within the first 12 hours, followed by a gradual decrease to near zero by 48 hours.*
FDA Label Image

Principal Display Panel (0.35 mg Tablet Blister Pack Pouch Label)

Principal Display Panel (0.35 mg Tablet Blister Pack Pouch Label)
A prescription label text panel for Norethindrone 0.35 mg, 28-day supply, labeled with directions to take one tablet by mouth daily. The text includes bilingual dosing instructions in English and Spanish, patient information fields, batch and lot numbers, expiration date, NDC number 76413-118-28, and labeler name Mylan. It restricts transfer by federal law.*

* 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.