Norethindrone
Product Images NDC 72789-439

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Norethindrone (NDC 72789-439). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pd-rx 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

72789439 Label (72789439)

72789439 Label (72789439)
Label for Norethindrone USP 0.35 MG oral tablets, 28 count, by PD-Rx Pharmaceuticals, Inc. The label includes the product name, strength, and quantity, NDC 72789-439-79, lot number J24E99, and expiration date 01/2028. It contains warnings to keep out of reach of children and storage instructions. The label also provides a contact number for reporting side effects.*
FDA Label Image

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

Structure (Dcc81f04 856f 46a8 998a 288a394d0092 01)
Chemical structure of Norethindrone, illustrating its steroidal core with attached hydroxyl, methyl, acetylene, and ketone functional groups.*
FDA Label Image

Instructions For Use Figure 1 (Image 02)

Instructions For Use Figure 1 (Image 02)
An instructional diagram for Norethindrone Tablets USP 0.35 mg showing a 28-tablet blister pack layout. The diagram includes arrows and text guiding patients where to start taking pills, depicting weekly rows labeled Sunday through Saturday. It instructs on day-1 starters and Sunday starters, indicating the pill-taking direction from left to right each week.*
FDA Label Image

Instructions For Use Figure 2 (Image 03)

Instructions For Use Figure 2 (Image 03)
An instructional diagram showing day labels for a weekly schedule, arranged in rows for Monday through Sunday, repeated in a pattern. It includes instructions for selecting the day label strip that corresponds with the first day of the menstrual period and aligning it with the blister pack days for proper use, noting that starting on Sunday requires no alignment step.*

* 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.