Product Images Ampicillin
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Product Label Images
The following 8 images provide visual information about the product associated with Ampicillin NDC 51662-1560 by Hf Acquisition Co Llc, Dba Healthfirst, 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.
This vial contains 2g of Ampicillin sodium USP equivalent to Ampicillin. The vial should be stored between 20°C and 25°C. Sterile water for the injection should be added before direct Intravenous use. The recommended adult dosage is between 250mg and 500mg every 6 hours, intravenously. For more information on indications, dosage, and precautions, refer to the accompanying insert. This product is manufactured in India and distributed by Ausromedics.*
This is a description of an injectable drug called "AMPICIL" in a vial size of 2 gm. The rest of the text seems to be product and batch information, including a code "a1 03 s02150025" and a prescription warning "RX ONLY".*
This is a dosage table showing the recommended dosage for bacterial meningitis and septicemia in neonates (less than or equal to 28 days of postnatal age). Dosage is based on gestational age and postnatal age, with different dosages recommended for different ranges. The highest recommended dosage is 150 mg/kg/day, administered in equally divided doses every 8 or 12 hours.*
This text appears to be a table with headers "Recommended Amount of Diluent", "Withdrawable Volume", and "Concentration (in mg/mL)". It lists four entries with different medication codes (55150-111-10, 55150-112-10, 55150-113-10, and 55150-114-20), corresponding recommended amounts of diluent, withdrawable volumes, and concentrations for different medication doses.*
This is a table displaying the stability periods of various diluent concentrations for a substance at room temperature (25°C) and in refrigerated conditions (4°C). The diluents used are Sterile Water for Injection, 0.9% Sodium Chloride Injection, USP, 5% Dextrose Injection, USP, 5% Dextrose and 0.45% Sodium Chloride Injection, USP, and Lactated Ringer's Injection, USP. The stability periods range from 1 to 72 hours depending on the diluent concentration and storage temperature.*
* 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.