Doxycycline Injection, Powder, Lyophilized, For Solution
Product Images NDC 70748-338

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Doxycycline (NDC 70748-338). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lupin Pharmaceuticals, 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

Carton Label (F239f903 F677 4be2 Bceb 3e59fbe1a079 01)

Carton Label (F239f903 F677 4be2 Bceb 3e59fbe1a079 01)
Packaging label for DOXYCYCLINE for Injection, USP 100 mg per vial, an intravenous lyophilized powder for solution by Lupin Pharmaceuticals, Inc. The label includes the product name, strength, route, NDC 70748-338-10, and states "Must be further diluted after reconstitution" and "Preservative free." The package contains 10 single-dose vials. Additional text includes storage instructions and manufacturer details. Dimensions of the packaging are also marked on the label layout.*

* 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.