Milrinone Lactate Injection, Solution
Product Images NDC 83301-0016
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Product Visual Gallery
This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Milrinone Lactate (NDC 83301-0016). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Mullan Pharmaceutical 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.
Milrinone 10ml (Milrinone 10mg 10ml Container Label 10.11.2023 With Barcode Small)
This is a description for Milrinone Lactate Injection, USP, which is used for intravenous use only. Each mL of the injection contains milfinone lactate equivalent to 1mg milfinone and 47mg Dextrose Anhydrous, USP, in Water for Injection, USP. The pH is adjusted between 3.2 and 4.0 with lactic acid or sodium hydroxide. The total concentration of lactic acid can vary between 0.95 mg/mL and 1.2 mg/mL. The injection does not contain a preservative, and any unused portion should be discarded after initial use. The usual dosage should be consulted in the package insert. The injection should be stored at 20° to 25°C (68° to 77°F) and should be protected from freezing. The product is manufactured by MULLAN Nulan Prarmaceutca Inc. in Fasatana, CA with a QR code. The manufacturing is done by Shandong New Tene Pharmaceutal Co in Feixian, Shandong, China. The lot and expiration date are not available.*
Milrinone-carton 20ml (Milrinone 20mg 20ml Carton Label 10.11.2023 With Barcode Small)
Milrinone-container 20ml (Milrinone 20mg 20ml Container Label 10.11.2023 With Barcode Small)
Milrinone Lactate is an injectable medication used for intravenous use only. It comes in a 20mg/20mL single dose vial. Each mL contains 1mg of milrinone and 47mg of Dextrose Anhydrous, USP, in Water for Injection, USP. The pH is adjusted between 3.2 and 4.0 with lactic acid or sodium hydroxide. This medication does not contain a preservative. Any unused portion should be discarded after initial use. The usual dosage should be determined based on the package insert. It should be stored between 20° and 25°C and should not be frozen. This medicine is manufactured by Spandong N Tine Prmaceutca Co in Feixian, Shandong, China for Nullan Pharmaceuticalnc in Pasadens, CA 91101. The lot number and expiration date are not available in the text.*
Structure (Structure)
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.