Moxifloxacin Hydrochloride
Product Images NDC 40032-034

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Moxifloxacin Hydrochloride (NDC 40032-034). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Novel Laboratories, 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

Structure (709f0134 B44a 4bed 9353 E6f0e5583c9e 01)

Chemical structure of Moxifloxacin Hydrochloride, showing its molecular arrangement including fluorine, oxygen, nitrogen, and hydrogen atoms with HCl indicated.*

FDA Label Image

Graph (709f0134 B44a 4bed 9353 E6f0e5583c9e 02)

Pharmacokinetic curve showing plasma concentration (µg/mL) of Moxifloxacin Hydrochloride over time (hours) comparing oral dose and intravenous (i.v.) dose. The graph displays concentration decreasing from peak levels within 24 hours post-dose.*

FDA Label Image

Container (709f0134 B44a 4bed 9353 E6f0e5583c9e 03)

Label for Moxifloxacin Hydrochloride Tablets 400 mg by Novel Laboratories, Inc. The label states the product contains 30 tablets and includes directions for dosage, storage instructions to keep at 20° to 25°C and avoid high humidity, and pharmacist dispensing advice. The NDC number 40032-034-03 and barcodes are also displayed.*

FDA Label Image

Blister (709f0134 B44a 4bed 9353 E6f0e5583c9e 04)

Label for Moxifloxacin Hydrochloride tablet, 400 mg, manufactured by Novel Laboratories, Inc., Somerset, NJ. The label shows the NDC number 40032-034-30, barcode, and spaces for expiration date and lot number. The image displays two identical label sections separated by a perforation line.*

FDA Label Image

Carton (709f0134 B44a 4bed 9353 E6f0e5583c9e 05)

Moxifloxacin Hydrochloride Tablets 400 mg unit-dose carton from Novel Laboratories, Inc. The label displays the active ingredient strength as 400 mg, the quantity as 50 unit-dose tablets, and includes instructions for pharmacists to dispense the accompanying Medication Guide. The storage recommendation is to keep the product between 20° to 25°C (68° to 77°F) and avoid high humidity. The manufacturer's information and barcode are also shown.*

* 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.