Vasopressin Injection
Product Images NDC 51662-1314

8 FDA label images from Hf Acquisition Co Llc, Dba Healthfirst · 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 51662-1314). 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 Vial (1314 1 Serialized Label On Labeled Vial)

Serialized Vial (1314 1 Serialized Label On Labeled Vial)
Vasostrict Vasopressin Injection USP 20 Units per mL vial for intravenous infusion. The label shows NDC 42023-164-01 and indicates it is Rx only. Distributed by HF Acquisition Co LLC, Mukilteo, WA. The image includes a GS1 barcode and manufacturing date code on an additional label adjacent to the vial.*
FDA Label Image

51662 1314 2 Pouch Labeling

51662 1314 2 Pouch Labeling
Label for Vasostrict (vasopressin injection, USP) 20 units per mL in a 1 mL vial. The label includes the NDC number 51662-1314-2, lot number, and expiration date 2025-01-01. It states intravenous infusion use, storage instructions between 2°C and 8°C, and that the vial may be held at room temperature up to 25°C for 12 months. Manufactured by HF Acquisition Co LLC in Mukilteo, WA.*
FDA Label Image

How Supplied-storage (How Supplied Storage)

How Supplied-storage (How Supplied Storage)
A storage and stability table for Vasopressin injection vials (1 mL and 10 mL). It details conditions for unopened refrigerated storage (2°C to 8°C/36°F to 46°F), unopened room temperature storage (20°C to 25°C/68°F to 77°F), and stability after opening. The 1 mL vial is stable until the manufacturer expiration date refrigerated, 12 months at room temperature, and no data for after opening. The 10 mL vial has similar unopened stability and is stable for 30 days after first puncture.*
FDA Label Image

Serialized Label (Serialized Label Only)

Serialized Label (Serialized Label Only)
A partial packaging label for Vasopressin 20 [USP'U]/mL injection by HF Acquisition Co LLC, DBA HealthFirst. The label includes a GS1 DataMatrix barcode, several identifier numbers, a note to see the manufacturer’s package insert, and distribution details from Mukilteo, WA. The label also shows 'RX ONLY' indicating prescription use.*
FDA Label Image

Serialized Labeling 51662 1314 2

Serialized Labeling 51662 1314 2
A small white rectangular label on a transparent sealed bag displaying a barcode and text including serialized product information and distribution details. The label states 'See manufacturer's package insert' and identifies the distributor as HF Acquisition Co., LLC, Mukilteo, WA 98275. The label also includes the text 'RX ONLY' vertically.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure diagram illustrating the peptide sequence of Vasopressin, showing amino acids cysteine, tyrosine, phenylalanine, glutamine, asparagine, proline, arginine, and glycine in order with numbered positions 1 through 9.*
FDA Label Image

Vial Back (Vial Label Back)

Vial Back (Vial Label Back)
Vasopressin 20 USP'U/mL injection vial with an orange cap. The clear glass vial has a white label with black text and a barcode, manufactured by HF Acquisition Co LLC, DBA HealthFirst. The vial is intended for intravenous use.*
FDA Label Image

Vial Front (Vial Label Front)

Vial Front (Vial Label Front)
Vasostrict (Vasopressin Injection, USP) 20 Units per mL in a 1 mL single-dose vial. The vial has a clear glass body with a white and orange label and an orange cap. It is intended for intravenous infusion and includes storage instructions. This product is labeled with NDC 42023-164-01.*

* 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.