Procainamide Hci Injection, Solution
Product Images NDC 51662-1334

10 FDA label images from Hf Acquisition Co Llc, Dba Healthfirst · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Procainamide Hci (NDC 51662-1334). 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

51662 1334 2 Serialized Pouch Label

51662 1334 2 Serialized Pouch Label
Label for PROCAINAMIDE HCl Injection, USP 100 mg/mL, 10 mL vial. The label shows the NDC 51662-1334-2 and details for intravenous or intramuscular use. It includes storage instructions, warnings about preservatives and sulfites, manufacturer information (HF Acquisition Co., LLC, Mukilteo, WA), and a QR code.*
FDA Label Image

51662 1334 3 Serialized Case Label

51662 1334 3 Serialized Case Label
Label for PROCAINAMIDE HCl Injection, USP 1 gram/10 mL (100 mg/mL) solution in a 10 mL vial, box of 25. It includes NDC 51662-1334-3, lot number 123456, and expiration date 2030-01-01. Manufactured by HF Acquisition Co LLC, Mukilteo, WA. Intended for intravenous or intramuscular use with warnings about preservatives and storage conditions.*
FDA Label Image

51662 1334 3 Serialized Case Labeling

51662 1334 3 Serialized Case Labeling
A label on white packaging showing a GS1 DataMatrix barcode and GS1 Application Identifiers (01, 17, 21, 10) with corresponding numeric values. The label notes the product is distributed by HF Acquisition Co., LLC, Mukilteo, WA 98275, and includes the text 'RX ONLY'. No product name, dosage form, or strength is visible.*
FDA Label Image

Box Label (Box Label)

Box Label (Box Label)
Label for PROCAINAMIDE HYDROCHLORIDE Injection, USP, 100 mg/mL (1 gram/10 mL total) in a 10 mL multiple-dose vial. The label includes warnings about preservatives like methylparaben and sodium metabisulfite, instructions for aseptic technique, storage conditions, and notes that the solution is sterile and nonpyrogenic for intramuscular or intravenous use. Manufactured by Hospira, Inc., Lake Forest, IL.*
FDA Label Image

D1 (Dosage And Administration)

D1 (Dosage And Administration)
A data table titled "DILUTIONS AND RATES FOR INTRAVENOUS INFUSIONS" for Procainamide Hydrochloride Injection, USP, presenting final concentrations, infusion volumes, procainamide hydrochloride amounts to be added, and infusion rates for initial loading and maintenance infusions. It includes notes on infusion volume preparation with 5% Dextrose Injection and warnings about monitoring infusion flow rates to avoid high plasma levels and hypotension.*
FDA Label Image

How Supplied (How Supplied)

How Supplied (How Supplied)
A data table listing two NDC numbers for fliptopp vials with concentrations and sizes: 100 mg/mL in a 10 mL vial and 500 mg/mL in a 2 mL vial.*
FDA Label Image
FDA Label Image

Serialized Box (Serialized Box)

Serialized Box (Serialized Box)
Packaging label for PROCAINAMIDE HYDROCHLORIDE Injection, USP, multiple-dose vial containing 1 gram per 10 mL total (100 mg/mL). The package shows a 10 mL vial, Rx only, distributed by Hospira, Inc., Lake Forest, IL. Label includes a warning that it contains metabisulfites.*
FDA Label Image

Structure (Structure Desc)

Structure (Structure Desc)
Chemical structure of Procainamide HCl showing the molecular composition with a benzene ring, amide group, diethylamino group, and hydrochloride component.*
FDA Label Image

Vial Label (Vial Label)

Vial Label (Vial Label)
Label for PROCAINAMIDE HCl Injection, USP 100 mg/mL, 10 mL multiple-dose vial. The label states 1 gram per 10 mL total, includes preservative methylparaben and sodium metabisulfite, with a warning about metabisulfites. Manufactured by Hospira, Inc.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.