Enalaprilat Injection
Product Images NDC 0143-9787

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Enalaprilat (NDC 0143-9787). 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

Chemical Structure (Enalaprilat Injection 1)

Chemical structure of enalaprilat showing its molecular composition and arrangement, including notation for two water molecules (2H2O).*

FDA Label Image

Enalaprilat Injection, Usp 1.25 mg/ml (Enalaprilat Injection 2)

Label for Enalaprilat Injection, USP, 1.25 mg/mL strength in a 1 mL single-use vial. The label includes storage instructions to keep at 25°C (77°F) with excursions permitted between 15° to 30°C (59° to 86°F). It is for intravenous use only, Rx only, and is labeled by Hikma Pharmaceuticals USA Inc.*

FDA Label Image

Enalaprilat Injection, Usp 2.5 mg/2 mL (Enalaprilat Injection 3)

Enalaprilat Injection USP 2.5 mg/2 mL (1.25 mg/mL) single-use vial label. The label includes storage instructions at 25°C with permitted excursions, manufacturer details Hikma Farmacêutica (Portugal) S.A., and distributor West-Ward Pharmaceutical Corp. The vial is for intravenous use only and is prescription-only.*

FDA Label Image

Enalaprilat Injection 4

A drug vial label for Enalaprilat injection by Hikma Pharmaceuticals USA Inc. The label includes a QR code and clear text fields for GTIN, serial number, expiration date, and lot number. No proprietary or strength information is visible beyond the product data provided.*

* 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.