Levofloxacin Injection, Solution
Product Images NDC 44567-435

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Levofloxacin (NDC 44567-435). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Wg Critical Care, 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.

FDA Label Image

Levofloxacin 500 mg Bag Label (Image 01)

This is a medication called Levofloxacin, which is available in 250mg in a 50mL solution of 5% Dextrose. It is recommended to infuse over 60 minutes after removing it from the overwrap, and no further dilution is necessary. The 50mL contains a dilute solution equivalent to 250mg of Levofloxacin. This medication should not be used in a series and the pharmacist should provide the medication guide to each patient. The manufacturer is WG Critical Care, LLC in Paramus, NJ, USA. The expiration date is unknown.*

FDA Label Image

Levofloxacin 750 mg Bag Label (Image 02)

This is the description of a medication called Levofloxacin, which is administered by infusion through injection in 5% Dextrose. The injection should be infused over 60 minutes once removed from the overwrap, and as necessary. The solution is diluted and contains 500mg of Levofloxacin in 8 corrose. It may also contain Hydrochionc Acd, NF, and/or Sodum Hydroxde, NF 10 adust 410 38 10 68. It is important to note that additives shall not be added or used simultaneously through the same venous line. The medication has been manufactured by WG Critical Care LLC and comes in a package size of 100 mL.*

FDA Label Image

Image 03

This is a medication with the NDC number 44567-437-24 and the volume of 150 mL. It is an injection of Levofloxacin, which is diluted in 5% Dextrose with a concentration of 750 mg (5 mg/mL). It should be infused over 90 minutes without further dilution. The solution has a pH of 10 381055 and may contain Hydrochloric Acid, NF and/or Sodium Hydroxide, NF to adjust the pH level. The additives should not be added or infused.*

FDA Label Image

Chemical Structure (Lev0b 0000 01)

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Figure 2 (Lev0b 0000 02)

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Figure 3 (Lev0b 0000 03)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.