Norepinephrine Bitartrate
Product Images NDC 47335-615

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Norepinephrine Bitartrate (NDC 47335-615). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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

Spl-norepinephrine-carton (Spl Norepinephrine Carton)

Label for Norepinephrine Bitartrate Injection, USP 4 mg/4 mL (1 mg/mL) sterile injection. The product comes in 10 single-dose fliptop vials of 4 mL each. It includes warnings about sulfites and administration precautions. Manufactured by Gland Pharma Limited and distributed by Sun Pharmaceutical Industries, Inc.*

FDA Label Image

Spl-norepinephrine-carton1 (Spl Norepinephrine Carton1)

Norepinephrine Bitartrate Injection, USP 4 mg/4 mL (1 mg/mL) label from Sun Pharmaceutical Industries, Inc. The label indicates a concentration of 1 mg norepinephrine base per mL and notes sodium chloride and sodium metabisulfite as components. It specifies storage instructions, usage warnings about solution discoloration, and comes in 10 single-dose 4 mL fliptop vials for intravenous infusion.*

FDA Label Image

Spl-norepinephrine-structure (Spl Norepinephrine Structure)

Chemical structure of norepinephrine bitartrate depicted as two molecular diagrams showing molecular groups including phenol rings, hydroxyl groups, amine group, and carboxyl groups with water of hydration.*

FDA Label Image

Spl-norepinephrine-vial (Spl Norepinephrine Vial)

Norepinephrine Bitartrate Injection, USP label from Sun Pharmaceutical Industries, Inc. The injectable solution is 4 mg per 4 mL (1 mg/mL) in a 4 mL single-dose fliptop vial. The label includes dilution and light protection instructions, a sulfite warning, and manufacturing details including NDC 47335-615-40.*

* 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.