Nicardipine Hydrochloride Injection, Solution
Product Images NDC 67184-0611
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Product Visual Gallery
This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Nicardipine Hydrochloride (NDC 67184-0611). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Qilu Pharmaceutical Co., Ltd., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Container Label (Nicardipine Hydrochloride Injection Usp 2)
This is a description of Nifedipine Hydrochloride Injection, USP with a concentration of 25 mg/10 mL. It is for intravenous use only and must be diluted before infusion. The medication comes in a single dose vial of 10 mL and should be stored at controlled room temperature, protected from light. The manufacturer is QILU Pharmaceutical (Hainan) Co., Ltd. It is important to discard any unused portion of the medication. The lot number and expiry date are also provided for tracking and safety purposes.*
Carton (Nicardipine Hydrochloride Injection Usp 3)
This text appears to be a label of an injectable medication called Nicardipine Hydrochloride Injection, USP, with a concentration of 25 mg per 10 mL (2.5 mg/mL). It is indicated for intravenous use only and must be diluted before infusion. The medication is manufactured by a company located in Greece and each milliliter of solution contains 2.5 mg of nicardipine hydrochloride. The product is buffered with sorbitol and citric acid. It should be stored between 20°C to 25°C, protected from light, and in the original carton until ready to use. The usual dosage should be determined following the instructions provided in the package insert.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.