Morphine Sulfate Injection
Product Images NDC 0641-6127

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Morphine Sulfate (NDC 0641-6127). 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

Chemical Structure (Morphine Sulfate Injection Anda 1)

Chemical structure of morphine sulfate pentahydrate (C17H19NO3 with H2SO4 and 5H2O) showing the molecular arrangement of morphine ions and sulfate and water molecules associated in the salt form.*

FDA Label Image

West-ward Logo (Morphine Sulfate Injection Anda 2)

Label for Morphine Sulfate Injection, USP 4 mg/mL single-dose vial by Hikma Pharmaceuticals USA Inc. It specifies intravenous use only, protection from light, and discard instructions if precipitated. The vial contains 1 mL of solution, and the label includes an NDC, barcode, lot, and expiration information fields.*

FDA Label Image

Ndc 0641-6125-01 Morphine Sulfate Inj., Usp 4 mg/ml Cii For Iv Use Only Rx Only 1 mL Single Dose Vial Protect From Light Do Not Use If Precipitated (Morphine Sulfate Injection Anda 3)

Label for Morphine Sulfate Injection, USP 4 mg/mL by Hikma Pharmaceuticals USA Inc. The label specifies it is for intravenous use only and includes a warning to protect from light. Pack contains 25 single-dose vials of 1 mL each. Storage instructions indicate to keep at 20° to 25°C and avoid freezing. Additional formulation and usage details are provided on the label.*

FDA Label Image

Ndc 0641-6125-25 Rx Only Morphine Sulfate Injection, Usp 4 mg/ml Cii For Intravenous Use Only 25 X 1 mL Single Dose Vials (Morphine Sulfate Injection Anda 4)

Label for Morphine Sulfate Injection, USP, 8 mg/mL strength, single dose vial for intravenous use. The label states use for IV only, instructions to protect from light, and discard if precipitated. Manufactured by Hikma Pharmaceuticals USA Inc. The vial contains 1 mL of solution.*

FDA Label Image

Ndc 0641-6126-01 Morphine Sulfate Inj., Usp 8 mg/ml Cii For Iv Use Only Rx Only 1 mL Single Dose Vial Protect From Light Do Not Use If Precipitated (Morphine Sulfate Injection Anda 5)

Morphine Sulfate Injection, USP 8 mg/mL intravenous injection vial label by Hikma Pharmaceuticals USA Inc. The label states the product is for intravenous use only, light sensitive, and contains 25 single-dose vials of 1 mL each. The label also provides composition and storage instructions.*

FDA Label Image

Ndc 0641-6126-25 Rx Only Morphine Sulfate Injection, Usp 8 mg/ml Cii For Intravenous Use Only 25 X 1 mL Single Dose Vials (Morphine Sulfate Injection Anda 6)

Label for Morphine Sulfate Injection, USP, 10 mg/mL strength, in a 1 mL single dose vial. The label indicates it is for intravenous use only, must be protected from light, and discarded if precipitated. The product is manufactured by Hikma Pharmaceuticals USA Inc.*

FDA Label Image

Ndc 0641-6127-01 Morphine Sulfate Inj., Usp 10 mg/ml Cii For Iv Use Only Rx Only 1 mL Single Dose Vial Protect From Light Do Not Use If Precipitated (Morphine Sulfate Injection Anda 7)

Morphine Sulfate Injection USP 10 mg/mL intravenous injection vial label by Hikma Pharmaceuticals USA Inc. The label includes dosage strength, handling instructions to protect from light, storage conditions (20° to 25°C), and cautions against discoloration or precipitates. The packaging is a 25 x 1 mL single-dose vial carton manufactured in Eatontown, NJ.*

FDA Label Image

Ndc 0641-6127-25 Rx Only Morphine Sulfate Injection, Usp 10 mg/ml Cii For Intravenous Use Only 25 X 1 mL Single Dose Vials (Morphine Sulfate Injection Anda 8)

A label panel displaying a QR code alongside printed data including GTIN 00301234567896, serial number 1234567890123, placeholder expiry date formatted as MMYYYY, and lot code ABCDE12345. No proprietary or dosage information is visible on this label segment.*

* 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.