Doxycycline Injection, Powder, Lyophilized, For Solution
Product Images NDC 68382-911

7 FDA label images from Zydus Pharmaceuticals Usa Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Doxycycline (NDC 68382-911). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zydus 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

Image (530f87fb C1d3 496f A350 A9621c1ae1cc 01)

Image (530f87fb C1d3 496f A350 A9621c1ae1cc 01)
Chemical structure of doxycycline including its hydrochloride, water, and ethanol components as a complex shown with molecular formula C22H24N2O8·HCl and associated molecules; molecular weight 1025.89 is noted.*
FDA Label Image

100 mg (530f87fb C1d3 496f A350 A9621c1ae1cc 02)

100 mg (530f87fb C1d3 496f A350 A9621c1ae1cc 02)
Label for Doxycycline for Injection, USP 100 mg per vial, lyophilized powder for intravenous infusion by Zydus Pharmaceuticals USA Inc. The single-dose vial is preservative-free and must be diluted before use. Storage instructions specify 20° to 25°C. The label includes manufacturer and distributor details along with handling precautions such as protecting from light and sunlight during infusion.*
FDA Label Image

Vial Label (530f87fb C1d3 496f A350 A9621c1ae1cc 03)

Vial Label (530f87fb C1d3 496f A350 A9621c1ae1cc 03)
Doxycycline for Injection, USP 100 mg per vial lyophilized powder for intravenous infusion. Single-dose vial, preservative free. Label includes storage instructions at 20°C to 25°C, manufacturer Cadila Healthcare Ltd., and distributor Zydus Pharmaceuticals USA Inc. Additional details note vial contains doxycycline hyclate equivalent to 100 mg doxycycline with ascorbic acid and mannitol, with warnings to protect from light and retain in carton until use.*
FDA Label Image

100 mg (530f87fb C1d3 496f A350 A9621c1ae1cc 04)

100 mg (530f87fb C1d3 496f A350 A9621c1ae1cc 04)
Doxycycline for Injection, USP 100 mg per vial powder for injection box packaging label. The label is for intravenous infusion and contains 10 single-dose vials. It is manufactured by Zydus Pharmaceuticals USA Inc. The label includes diluting instructions and storage information. The NDC is 68382-910-10.*
FDA Label Image

Carton Label (530f87fb C1d3 496f A350 A9621c1ae1cc 05)

Carton Label (530f87fb C1d3 496f A350 A9621c1ae1cc 05)
Packaging label for Doxycycline for Injection, USP 100 mg per vial, powder for reconstitution for intravenous use. The label indicates a package containing 10 single-dose vials. It is manufactured by Zydus Pharmaceuticals USA Inc. The label includes drug identity, strength, usage route, and handling instructions.*
FDA Label Image

200 mg (530f87fb C1d3 496f A350 A9621c1ae1cc 06)

200 mg (530f87fb C1d3 496f A350 A9621c1ae1cc 06)
Label for Doxycycline for Injection, USP 200 mg per vial, lyophilized powder for intravenous infusion. Manufactured by Cadila Healthcare Limited, India, distributed by Zydus Pharmaceuticals USA Inc. The single-dose vial is preservative-free and must be diluted before use. Storage at 20 to 25°C is indicated. Label includes dosage, storage, and handling instructions.*
FDA Label Image

200 mg (530f87fb C1d3 496f A350 A9621c1ae1cc 07)

200 mg (530f87fb C1d3 496f A350 A9621c1ae1cc 07)
Carton packaging label for Doxycycline for Injection, USP 200 mg per vial, a single-dose vial for intravenous infusion. The lyophilized powder requires reconstitution before use. Labeler is Zydus Pharmaceuticals USA Inc. The label includes usage instructions, storage information, and manufacturer details (Cadila Healthcare Limited, India).*

* 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.