Fortaz
Product Images NDC 52565-106

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Fortaz (NDC 52565-106). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Teligent Pharma, 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

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Chemical structure of the active ingredient in FORTAZ by Teligent Pharma, Inc., depicting its molecular configuration with elements including nitrogen, oxygen, carbon, sulfur, and hydrogen atoms arranged in a complex ring and side chain formation.*

FDA Label Image

Fortaz 1g Vial Pdp

FORTAZ 1 g/Vial (ceftazidime for injection) label by Teligent Pharma, Inc. The label indicates the product strength as 1 gram per vial of anhydrous ceftazidime for injection, intended for intramuscular or intravenous use. It includes storage, handling instructions, lot, and expiration information.*

FDA Label Image

Fortaz 2g Vial Pdp

Label for Fortaz 2 g/vial (ceftazidime for injection) by Teligent Pharma, Inc. It shows the NDC number 52565-107-01 and indicates the product is for intravenous use only. The label includes storage and preparation instructions, lot and expiration placeholders, and barcodes.*

FDA Label Image

Fortaz 500mg

Label for FORTAZ (ceftazidime for injection) 500 mg vial from Teligent Pharma, Inc. The label includes dosage form and strength, NDC number 52565-105-01, usage instructions for intramuscular or intravenous use, storage conditions, manufacturer information, and barcodes. It also notes that the vial contains 59 mg of sodium carbonate and provides a caution on reconstitution and storage.*

* 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.