Phenylephrine Hydrochloride Injection
Product Images NDC 0641-6142

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Phenylephrine Hydrochloride (NDC 0641-6142). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hikma Pharmaceuticals Usa Inc., 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

Structural Formula (Phenylephrine Hydrochloride Injection Usp Nda 1)

Chemical structure diagram of Phenylephrine Hydrochloride showing the molecular arrangement with hydroxyl, amine, and phenyl groups along with the hydrochloride salt.*

FDA Label Image

West-ward Logo (Phenylephrine Hydrochloride Injection Usp Nda 2)

Label for Phenylephrine Hydrochloride Injection USP 10 mg/mL by Hikma Pharmaceuticals USA Inc. The label indicates the product is for intravenous use and comes as a 1 mL single dose vial. Instructions include dilution before use and protection from light. The label displays NDC 0641-6142-01 along with lot and expiration information areas.*

FDA Label Image

Ndc 0641-6142-01 Phenylephrine HCl Injection, Usp 10 mg/ml For Intravenous Use Dilute Before Use 1 mL Single Dose Vial Discard Unused Portion Protect From Light (Phenylephrine Hydrochloride Injection Usp Nda 3)

Label for Phenylephrine Hydrochloride Injection USP 10 mg/mL, for intravenous use. The label indicates it is a single-dose vial, with instructions to dilute before use and discard unused portion. It includes storage instructions to protect from light and keep covered until use. Manufactured by Hikma Pharmaceuticals USA Inc.*

FDA Label Image

Ndc 0641-6142-25 Rx Only Phenylephrine HCl Injection, Usp 10 mg/ml For Intravenous Use Dilute Before Use 25 X 1 mL Single Dose Vials Discard Unused Portion (Phenylephrine Hydrochloride Injection Usp Nda 4)

Phenylephrine Hydrochloride Injection, USP 10 mg/mL (50 mg/5 mL) vial by Hikma Pharmaceuticals USA Inc. Label indicates the product is for intravenous use, prescription only, and must be diluted before use. The vial contains 5 mL, features storage instructions, and a barcode is visible on the label.*

FDA Label Image

Phenylephrine Hydrochloride Injection Usp Nda 5

Phenylephrine Hydrochloride Injection, USP 10 mg/mL (50 mg/5 mL) is an intravenous injection labeled for prescription use. The label indicates a pharmacy bulk package not for direct infusion, containing 10 vials of 5 mL each. It is manufactured by Hikma Pharmaceuticals USA Inc. The label includes storage instructions and a barcode.*

FDA Label Image

Phenylephrine Hydrochloride Injection Usp Nda 6

Label for Phenylephrine Hydrochloride Injection USP, 100 mg/10 mL (10 mg/mL) intravenous injection by Hikma Pharmaceuticals USA Inc. The label states it is a pharmacy bulk package, not for direct infusion, must be diluted, and protected from light. It includes active ingredients, storage instructions (20° to 25°C), and directions for use to see the package insert. The vial volume is 10 mL.*

FDA Label Image

Phenylephrine Hydrochloride Injection Usp Nda 7

Phenylephrine Hydrochloride Injection, USP 100 mg/10 mL (10 mg/mL) vial label. It is indicated for intravenous use and must be diluted. The label states it is a pharmacy bulk package not for direct infusion and contains 10 vials of 10 mL each. Manufactured by Hikma Pharmaceuticals USA Inc. Storage instructions and active ingredient details are included.*

FDA Label Image

Phenylephrine Hydrochloride Injection Usp Nda 8

Label of Phenylephrine Hydrochloride injection showing a QR code, GTIN (00301234567896), serial number, expiration date placeholder (MMYYYY), and lot number (ABCD12345). The label is from Hikma Pharmaceuticals USA 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.