Vasopressin Injection
Product Images NDC 51662-1623

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Vasopressin (NDC 51662-1623). 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

Serialized Label (51662 1623 1 Serialized Rfid Label)

Serialized Label (51662 1623 1 Serialized Rfid Label)
The image shows a section of the Vasopressin injection packaging label from HF Acquisition Co LLC, DBA HealthFirst. It includes an encoded data matrix barcode and nearby text with identifiers including GS1 application identifiers and batch/lot number information. The label instructs to see the manufacturer's package insert and indicates the product is distributed by HF Acquisition Co, LLC in Mukilteo, WA.*
FDA Label Image

Vial Label (51662 1623 1 Vial Label)

Vial Label (51662 1623 1 Vial Label)
Label for Vasopressin Injection, USP, 20 Units per mL, 1 mL multiple dose vial for intravenous infusion. Manufactured in India for AuroMedics Pharma LLC, East Windsor, NJ. Includes storage instructions between 2°C and 8°C, dosage guidance to see full prescribing information, and usage instructions after initial vial entry. Contains batch and expiry placeholders.*
FDA Label Image

Pouch (51662 1623 2 Serialized Pouch Labeling)

Pouch (51662 1623 2 Serialized Pouch Labeling)
Label for Vasopressin Injection USP 20 Units per mL in a 1 mL vial, manufactured by HF Acquisition Co LLC. The label includes the NDC 51662-1623-2, lot number, and expiration date. Storage instructions and usage precautions for intravenous infusion are also visible.*
FDA Label Image

Serialized Rfid Pouch Labeling (51662 1623 2 Serialized Rfid Labeling)

Serialized Rfid Pouch Labeling (51662 1623 2 Serialized Rfid Labeling)
A label for Vasopressin injection, distributed by HF Acquisition Co., LLC. The label includes a barcode and several numeric codes, along with a note to see the manufacturer's package insert. The text also indicates "RX ONLY."*
FDA Label Image

Structure (Description)

Structure (Description)
Chemical structure diagram showing the amino acid sequence of vasopressin with residues numbered from 1 to 9, including cysteine, tyrosine, phenylalanine, glutamine, aspartic acid, proline, arginine, and glycine.*
FDA Label Image

Dosage (Dosage)

Dosage (Dosage)
A table titled 'Table 1 Preparation of diluted solutions' showing how to prepare diluted vasopressin injection solutions with and without fluid restriction. It includes columns for fluid restriction status, final concentration, and mix volumes of vasopressin injection and diluent.*
FDA Label Image

Storage And Handling (How Supplied Storage)

Storage And Handling (How Supplied Storage)
A storage and expiration table for VASOPRESSIN 20 USP'U/mL injection (1 mL vial) indicating recommended conditions and durations: unopened refrigerated at 2°C to 8°C (36°F to 46°F) until manufacturer expiration date; unopened room temperature at 20°C to 25°C (68°F to 77°F) for 12 months or until manufacturer expiration date, whichever is earlier; and opened (after first puncture), use within 48 hours.*
FDA Label Image

Vial Label (Vial Label 1623 2)

Vial Label (Vial Label 1623 2)
Vasopressin Injection, USP 20 Units per mL label for intravenous infusion in a 1 mL multiple dose vial. Manufactured by AuroMedics Pharma LLC. Includes storage instructions, dosage advisory, and space for batch and expiry dates. The label also features the NDC 55150-370-01 barcode and handling information.*

* 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.