Product Images Furosemide
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Product Label Images
The following 9 images provide visual information about the product associated with Furosemide NDC 51662-1336 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.
Furosemide Injection is a medication used for intravenous or intramuscular use. It comes in a 4mL vial, containing 40mg/4mL (10mg/mL). Each vial has an NDC code of 51662-1336-2, a lot number of ABCDEFGHIJKLMNOPQRST, and an expiration date of 2021-06-01. The medication should not be used if the solution appears discolored or contains particulate. It should be stored at a temperature range of 20 to 25C (68 to 77F) and protected from light. Any unused portions of the medication should be discarded. The product is distributed by HF Acquisition Co., LLC, based in Mukilteo, WA. The original manufacturer's NDC code is 0409-6102-18. Please refer to the manufacturer's package insert for detailed information.*
This appears to be a serial number and various codes for a medical product. The text recommends referring to the manufacturer's package insert and indicates that it is distributed by HF Acquisition Co., LLC in Washington state. The product is only intended for use with a prescription (Rx Only).*
This is a description for AV Honzv [T ยป]z Injection, USP with a concentration of 40mg/4mL. It comes in a vial size of 4mL with a box of 25. The National Drug Code (NDC) is 51662-1336-3 and the lot number is ABCDEFGHIJKLMNOPQRST with an expiration date of June 1, 2021. It is intended for intravenous or intramuscular use only, and it should not be used if the solution is discolored or contains particulate. It should be stored at 20 to 25C (68 to 77F), protected from light, and discarded if any unused portion remains. This drug is prescription only and the manufacturer's package insert should be consulted. It was originally made by NDC 0409-6102-18 and distributed by HF Acquisition Co., LLC in Mukilteo, WA 98275.*
The text describes different Units of Sale for a medication, including its Concentration, NDC code, and packaging details such as the number of vials or syringes per carton/bundle. There are multiple variations of the medication available with different concentrations and packaging options.*
This is a description of an injection medication manufactured by Hospira, Inc. The medication is contained in a single-use vial with a volume of 4 mL and is intended for intravenous or intramuscular use only under prescription. The National Drug Code (NDC) for the medication is 0409-6102-18. The medication contains 40 mg/4 mL (10 mg/mL) of Injection, USP RL-4984. The label warns not to use the medication if the solution appears discolored or contains particulate. The Lot/Exp number is not available in the given text.*
* 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.