Progesterone Injection
Product Images NDC 0143-9725

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Progesterone (NDC 0143-9725). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hikma Pharmaceuticals Usa 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

Progesterone Structural Formula. (Progesterone Injection 1)

Chemical structure diagram of Progesterone showing its steroid backbone with labeled methyl groups and keto functional groups. The molecular framework includes four fused rings characteristic of steroid hormones.*

FDA Label Image

Progesterone Injection, Usp 500 mg/10 mL (Progesterone Injection 2)

Label for Progesterone Injection USP 500 mg/10 mL (50 mg/mL) in a 10 mL multiple dose vial. The label indicates the product contains progesterone 50 mg per mL with benzyl alcohol 10% as preservative in sesame oil. It is sterile, for intramuscular use only, and labeled for prescription use (RX only). The labeler is Hikma Pharmaceuticals USA Inc. Storage instructions include keeping at 20° to 25°C and avoiding excessive heat.*

FDA Label Image

Progesterone Injection, Usp 500 mg/10 mL (Progesterone Injection 3)

Packaging label for Progesterone injection USP, 500 mg/10 mL (50 mg/mL), sterile, for intramuscular use. The label indicates a 10 mL multiple dose vial. Manufactured by Hikma Farmaceutica (Portugal) and distributed by West-Ward Pharmaceuticals USA Inc. The label includes storage instructions, dosage form, use restriction (Rx only), and NDC 0143-9725-01.*

FDA Label Image

Progesterone Injection 4

The image shows a label for Progesterone injection 50 mg/1 mL, by Hikma Pharmaceuticals USA Inc. It features a QR code and printed identifiers including GTIN, serial number, expiration date, and lot number in a standardized format.*

* 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.