Hydroxyprogesterone Caproate
Product Images NDC 47335-037

2 FDA label images from Sun Pharmaceutical Industries, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Hydroxyprogesterone Caproate (NDC 47335-037). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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

Spl-hydroxyprogesterone-caproate-figure-1 (Spl Hydroxyprogesterone Caproate Figure 1)

Spl-hydroxyprogesterone-caproate-figure-1 (Spl Hydroxyprogesterone Caproate Figure 1)
A line graph titled 'Proportion of Women Remaining Pregnant as a Function of Gestational Age' comparing Hydroxyprogesterone caproate and control groups. The y-axis shows the proportion remaining pregnant from 0 to 100%, and the x-axis shows gestational age at delivery in weeks from 16 to 42. Two curves depict pregnancy continuation rates for Hydroxyprogesterone caproate and control groups. Below the graph, a table lists the number of women at risk at each gestational week for both groups.*
FDA Label Image

Spl-hydroxyprogesterone-caproate-showbox (Spl Hydroxyprogesterone Caproate Showbox)

Spl-hydroxyprogesterone-caproate-showbox (Spl Hydroxyprogesterone Caproate Showbox)
Packaging label for Hydroxyprogesterone Caproate Injection 1,250 mg/5 mL (250 mg/mL) by Sun Pharmaceutical Industries, Inc. The label indicates it is for intramuscular use, provided in a 5 mL multidose vial, Rx only, sterile. Storage instructions, ingredient details, and manufacturer information are included, along with the NDC 47335-037-40 barcode.*

* 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.