Product Images Tobramycin

View Photos of Packaging, Labels & Appearance

Product Label Images

The following 8 images provide visual information about the product associated with Tobramycin NDC 0409-3578 by Hospira, Inc., such as packaging, labeling, and the appearance of the drug itself. This resource could be helpful for medical professionals, pharmacists, and patients seeking to verify medication information and ensure they have the correct product.

Logo - tobramycin 01

Logo - tobramycin 01

structural formula tobramycin sulfate - tobramycin 02

structural formula tobramycin sulfate - tobramycin 02

graphic reduced dosage nomogram - tobramycin 03

graphic reduced dosage nomogram - tobramycin 03

This text appears to be a chart displaying a reduced dosage nomogram for medication administration. The chart lists creatinine clearance values (in mL/min/1.73 m?) and corresponding percentages of normal, with recommended dosages from Table 3. Additionally, the chart includes serum creatinine values in mg/100 mL. The scales have been adjusted to facilitate dosage calculations.*

Logo - tobramycin 04

Logo - tobramycin 04

label ndc 0409-3577-01 - tobramycin 05

label ndc 0409-3577-01 - tobramycin 05

This is a description for a medicine that comes in a multiple-dose 2mlL container, with a National Drug Code (NDC) identification of 0409-3577-11. It is a pediatric prescription with a concentration of 20 mg/2 mL (10 mg/mL) and contains sulfites. It is labeled for LV or IM use, and it must be diluted for IV use. The medicine is distributed by Hospira, Inc. in Lake Forest, IL 60045 USA. The rest of the text is not relevant to the description.*

PRINCIPAL DISPLAY PANEL - 20 mg/2 mL Vial Tray - tobramycin 06

PRINCIPAL DISPLAY PANEL - 20 mg/2 mL Vial Tray - tobramycin 06

This is a label for a 20 mg/2 mL vial of medication that is intended for intramuscular or intravenous use. Dilution is necessary for intravenous use. The medication has been manufactured by Hospira, Inc, based in the United States and contains sulfites. The label also includes a barcode and product codes, but it is not clear what these codes are for.*

label ndc 0409-3578-01 - tobramycin 07

label ndc 0409-3578-01 - tobramycin 07

This is a medication with the brand name Tobramycinf#s, containing 80mg/2mL of an active ingredient that needs to be diluted for V use. It should be used with caution by individuals with sulfite allergies. The medication is distributed by Hospira, Inc. located in Lake Forest, IL, USA. There are several reference numbers on the packaging, including a National Drug Code (NDC) of 0409-3578-11, and other identifiers like FP0, 7.5 Mil, RL-7492, and HHE-HH#H-AA, which may be used for tracking and inventory purposes. The text also contains a warning and instructions to use the medicine for LV or M use only while also providing a prescription note.*

PRINCIPAL DISPLAY PANEL - 80 mg/2 mL Vial Tray - tobramycin 08

PRINCIPAL DISPLAY PANEL - 80 mg/2 mL Vial Tray - tobramycin 08

This appears to be a description of a medication in the form of an injection with a NDC (National Drug Code) number of 0409-3578-01. The injection is made in Hungary and distributed by Hospira, Inc. in the USA. The text includes a note that the medication must be diluted for intravenous use and is only available by prescription. There is also mention of a multiple-dose vial. The rest of the text is not legible and appears to be garbled.*

* The product label images have been analyzed using a combination of traditional computing and machine learning techniques. It should be noted that the descriptions provided may not be entirely accurate as they are experimental in nature. Use the information in this page at your own discretion and risk.