Estradiol Valerate Injection
Product Images NDC 0143-9290

8 FDA label images from Hikma Pharmaceuticals Usa Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Estradiol Valerate (NDC 0143-9290). 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

Structure (Estradiol Valerate Injection Usp 1)

Structure (Estradiol Valerate Injection Usp 1)
Chemical structure diagram of Estradiol Valerate, depicting its molecular framework with labeled atoms and bonds corresponding to the compound's steroid backbone and valerate ester group.*
FDA Label Image

50 mg Per 5 mL Container (Estradiol Valerate Injection Usp 2)

50 mg Per 5 mL Container (Estradiol Valerate Injection Usp 2)
Label for Estradiol Valerate Injection, USP, 50 mg per 5 mL (10 mg/mL) by Hikma Pharmaceuticals USA Inc. The label indicates a 5 mL multiple dose vial for intramuscular use only, sterile, with a list of inactive ingredients and storage instructions.*
FDA Label Image

100 mg Per 5 mL Container (Estradiol Valerate Injection Usp 3)

100 mg Per 5 mL Container (Estradiol Valerate Injection Usp 3)
Packaging label for Estradiol Valerate Injection, USP, 10 mg/mL (50 mg per 5 mL) multiple dose vial by Hikma Pharmaceuticals USA Inc. The label states intramuscular use only, sterile, and includes storage instructions (20° to 25°C). It lists the active ingredient with its concentration and preservatives, and provides manufacturer and distributor information along with barcode and NDC 0143-9289-01.*
FDA Label Image

200 mg Per 5 mL Container (Estradiol Valerate Injection Usp 4)

200 mg Per 5 mL Container (Estradiol Valerate Injection Usp 4)
Estradiol Valerate Injection, USP 100 mg per 5 mL (20 mg/mL) in a 5 mL multiple dose vial by Hikma Pharmaceuticals USA Inc. The label specifies intramuscular use only and lists inactive ingredients including benzyl benzoate and benzyl alcohol. The vial is sterile and for human prescription use.*
FDA Label Image

Estradiol Valerate Injection Usp 5

Estradiol Valerate Injection Usp 5
Packaging label for Estradiol Valerate Injection, USP 100 mg per 5 mL (20 mg/mL) by Hikma Pharmaceuticals USA Inc. The label indicates a 5 mL multiple dose vial, sterile and for intramuscular use only. It includes storage instructions (20° to 25°C), ingredients details, NDC 0143-9290-01, manufacturer information from Portugal, and a barcode.*
FDA Label Image

Estradiol Valerate Injection Usp 6

Estradiol Valerate Injection Usp 6
Label for Estradiol Valerate Injection, USP 200 mg per 5 mL (40 mg/mL) intramuscular injection in a 5 mL multiple dose vial. The label states it is sterile and for intramuscular use only. The labeler is Hikma Pharmaceuticals USA Inc. Additional storage and ingredient information is included.*
FDA Label Image

Estradiol Valerate Injection Usp 7

Estradiol Valerate Injection Usp 7
Packaging label for Estradiol Valerate Injection, USP 40 mg/mL (200 mg per 5 mL) by Hikma Pharmaceuticals USA Inc. The label indicates a 5 mL multi-dose vial for intramuscular use only. It includes storage instructions and lists inactive ingredients such as benzyl benzoate and castor oil. The label also displays the NDC code 0143-9291-01 and barcode.*
FDA Label Image

Estradiol Valerate Injection Usp 8

Estradiol Valerate Injection Usp 8
A rectangular product label for Estradiol Valerate injection from Hikma Pharmaceuticals USA Inc. The label includes a QR code on the left side and text on the right listing GTIN, serial number (SN), expiration date (EXP), and lot number (LOT) placeholders.*

* 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.