Doxycycline Injection, Powder, Lyophilized, For Solution
Product Images NDC 70121-1616

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Doxycycline (NDC 70121-1616). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals 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.

Product Images & Figures Index

FDA Label Image

1 (Doxycycline For Injection Usp 1)

1 (Doxycycline For Injection Usp 1)
Chemical structure diagram of doxycycline hydrochloride ethanol hydrate showing molecular groups and bonds, consistent with the lyophilized powder for injection formulation.*
FDA Label Image

Vial (Doxycycline For Injection Usp 2)

Vial (Doxycycline For Injection Usp 2)
Label for Doxycycline for Injection, USP, 100 mg per vial, a lyophilized powder for intravenous infusion by Amneal Pharmaceuticals LLC. The single-dose vial must be further diluted after reconstitution. The label includes storage instructions, preservative-free status, and barcodes, along with manufacturer details.*
FDA Label Image

Carton (Doxycycline For Injection Usp 3)

Carton (Doxycycline For Injection Usp 3)
Carton label for Doxycycline for Injection, USP 100 mg per vial by Amneal Pharmaceuticals LLC. The label specifies it is an intravenous injection, powder lyophilized for solution, preservative-free, and must be further diluted after reconstitution. The package contains 10 single-dose vials. Manufacturer information and usage instructions are also included on the label.*

* 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.