Medroxyprogesterone Acetate Tablet
Product Images NDC 70518-4777

3 FDA label images from Remedyrepack Inc. · 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 Medroxyprogesterone Acetate (NDC 70518-4777). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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.

Product Images & Figures Index

FDA Label Image

Fig1 (Image 1)

Fig1 (Image 1)
Chemical structure of Medroxyprogesterone Acetate as shown in the image, depicting its molecular arrangement with carbon (C), hydrogen (H), and oxygen (O) atoms in the steroidal backbone and ester functional groups.*
FDA Label Image

Mm1 (Medroxyprogesterone Acetate 5mg 70518 4777 00)

Mm1 (Medroxyprogesterone Acetate 5mg 70518 4777 00)
Medroxyprogesterone Acetate 5 mg tablet label shows a quantity of 100 tablets per box. The label indicates the product is repackaged by RemedyRepack Inc., Indiana, PA. Storage instructions specify keeping the product at 20-25°C with permitted excursions. The label includes a QR code, partial manufacturer information (Teva, Frazer, PA), and typical warnings to keep out of children's reach.*
FDA Label Image

Remedy_label (Remedy Label)

Remedy_label (Remedy Label)
Label for Medroxyprogesterone Acetate 5 mg tablet, oral dosage form. The label indicates a quantity of 1 tablet with NDC number 70518-4777-01. It is repackaged by RemedyRepack Inc., Indiana, PA. Additional details include storage instructions and manufacturer information noting Teva, Frazer, PA.*

* 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.