Terbutaline Sulfate Injection
Product Images NDC 71872-7080

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Terbutaline Sulfate (NDC 71872-7080). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Medical Purchasing Solutions. Llc, 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

Pdp (7080)

Label for Terbutaline Sulfate Injection USP 1 mg/mL in a 1 mL single dose vial. The label provides product information including sterile, nonpyrogenic aqueous solution for subcutaneous injection, manufacturer HIKMA Pharmaceuticals, and repackager Medical Purchasing Solutions, Scottsdale, AZ. It includes dosage instructions and storage conditions, emphasizing the vial is intended for single patient use.*

FDA Label Image

Terbutaline Sulfate Structure (Terbutaline Sulfate Injection 1)

Chemical structure of Terbutaline Sulfate showing the molecular arrangement including hydroxyl groups, aromatic ring, and sulfate ions.*

FDA Label Image

Terbutaline Sulfate Injection, Usp 1 mg/ml For Subcutaneous Use Only (Terbutaline Sulfate Injection 2)

Terbutaline Sulfate Injection, USP 1 mg/mL single-dose vial label for subcutaneous use only. The label includes storage instructions of 20°C to 25°C (68°F to 77°F), USP controlled room temperature, and advises protecting from light. Manufactured by Hikma Pharmaceuticals and distributed by West-Ward Pharmaceutical Corp. The label features dosage form, strength, and usage directions prominently.*

* 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.