Hydralazine Hydrochloride Injection, Solution
Product Images NDC 51662-1648

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Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Hydralazine Hydrochloride (NDC 51662-1648). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hf Acquisition Co Llc, Dba Healthfirst, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Pouch Label (51662 1648 2 Pouch)

Pouch Label (51662 1648 2 Pouch)
This is information for Hydralazine hydrochloride injection, USP28mg/mL 1mL Vial, intended for intramuscular or intravenous use in emergency situations for patients who are unable to take oral medication. Each ml contains Hydralazine hydrochloride 20mg, Propylene glycol 103.6mg, Methylparaben 0.65mg, Propylparaben 0.35mg, and Water for injection. It is sterile and nonpyrogenic, with a pH of the solution between 3.4 - 4.4 and may be adjusted if needed. The medication should be stored between 20 - 25ºC (68-77ºF). For detailed directions on usage, refer to the package insert. It is manufactured by HF Acquisition Co., LLC in Mukilteo, WA 98275.*
FDA Label Image

Case Label (51662 1648 3 Case)

Case Label (51662 1648 3 Case)
This is a description of a pharmaceutical product called HYDRALAZINE HYDROCHLORIDE INJECTION, USP. This product comes in vials containing 20mg/mL of solution, with each vial holding 1mL. Each case contains 25 vials. The medication is for intramuscular or intravenous use and is designed for emergency use in patients who cannot take oral medication. The ingredients in each mL include Hydralazine Hydrochloride (20mg), Propylene Glycol (183.6mg), Methylparaben (0.65mg), Propylparaben (0.35mg), and water for injection. The solution has a pH range of 3.4-4.4 and can be adjusted if needed. It is a sterile, nonpyrogenic product. Unused portions should be discarded, and it should be stored at 20-25°C. Refer to the package insert for directions for use. The product is manufactured by HFAcquisitionCo., LLC in Mukilteo, WA 98275. Original manufacturer NDC: 8517-8981-25.*
FDA Label Image

Rfid Label (51662 1648 3 Rfid)

Rfid Label (51662 1648 3 Rfid)
This text contains a unique identification number along with a manufacturer's package insert disclaimer. The product is distributed by HF Acquisition Co., LLC located in Mukilteo, WA 98275, and is intended for prescription use only.*
FDA Label Image

Structure (Structure 51662 1648)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.