Propranolol Hydrochloride Injection
Product Images NDC 51662-1338

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Propranolol Hydrochloride (NDC 51662-1338). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hf Acquisition Co Llc, Dba Healthfirst, 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

Labeled Vial (Labeled Vial)

The image shows a brown glass vial with a white cap labeled as PROPRANOLOL HYDROCHLORIDE Injection, USP. The concentration is 1 mg/mL. The label indicates the product is for intravenous use only and includes storage instructions. The vial is from the labeler HF Acquisition Co LLC, DBA HealthFirst.*

FDA Label Image

Serialized Vial (Serialized Vial)

The image shows an amber glass vial with a white cap labeled PROPRANOLOL HYDROCHLORIDE injection, USP. The label indicates a strength of 1 mg/mL and specifies it is for intravenous use only. Attached is a white informational tag with a barcode and manufacturing details, mentioning distribution by HF Acquisition Co., LLC.*

FDA Label Image

Structure (Structure)

Chemical structure of Propranolol Hydrochloride, showing its characteristic naphthalene ring system connected to an oxypropanolamine side chain and associated with a hydrochloride (HCl) group.*

FDA Label Image

Vial Label (Vial Label)

Label for PROPRANOLOL HYDROCHLORIDE Injection USP, 1 mg/mL in a 1 mL single-dose vial. The label indicates intravenous use only and shows storage instructions at 20°C to 25°C (68°F to 77°F). Manufactured by Hikma Farmacêutica (Portugal) and distributed by West-Ward Pharmaceutical Corp, Eatontown, NJ. Includes an NDC barcode and lot/expiration date fields.*

* 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.