Morphine Sulfate Injection
Product Images NDC 0641-6192

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Morphine Sulfate (NDC 0641-6192). 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

The Chemical Name Of Morphine Sulfate Is 7,8-didehydro-4,5-epoxy-17-methyl-(5α,6α)-morphinan-3,6-diol Sulfate (2:1) (salt), Pentahydrate, With The Following Structural Formula: (Morphine Sulfate Injection Usp Syringes 1)

Chemical structure of morphine sulfate, showing the molecular formula with sulfate and water of hydration components (H2SO4 and 5H2O). The diagram includes detailed atomic bonds and ring structures characteristic of morphine sulfate.*

FDA Label Image

Fig 1 (Morphine Sulfate Injection Usp Syringes 2)

An instructional diagram showing a syringe for Morphine Sulfate injection, highlighting parts labeled as Syringe Tip Cap (to be removed), External Collar (do not remove), Label displaying 1 mL Single Dose Syringe, and Plunger Rod. The image illustrates components of the intravenous injection device.*

FDA Label Image

Figure 2 (Morphine Sulfate Injection Usp Syringes 3)

An instructional illustration showing two hands handling an injection device or syringe. One hand is holding the syringe barrel while the other hand twists the cap or plunger, indicated by a curved arrow pointing clockwise, demonstrating how to open or prepare the injection.*

FDA Label Image

Ndc 0641-6191-01 Rx Only 1 mL Single-dose Prefilled Syringe 462-858-00 Morphine Sulfate Injection, Usp 2 mg/ml For Iv Use Only (Morphine Sulfate Injection Usp Syringes 4)

Label for Morphine Sulfate Injection, USP 2 mg/mL in a 1 mL single-dose prefilled syringe for intravenous use. The label includes dosage strength, route, NDC 0641-6191-01, Rx only status, and the labeler Hikma Pharmaceuticals USA Inc. It also displays lot number, expiration date, barcode, and a QR code.*

FDA Label Image

Ndc 0641-6191-10 Rx Only Morphine Sulfate Injection, Usp 2 mg/ml For Intravenous Use Only No Added Preservative 10 X 1 mL Single-dose Prefilled Syringes Discard Unused Portion. (Morphine Sulfate Injection Usp Syringes 5)

Morphine Sulfate Injection, USP 2 mg/mL for intravenous use ONLY, labeled for human prescription. The carton is for 10 x 1 mL single-dose prefilled syringes with no added preservative. Manufactured by Hikma Pharmaceuticals USA Inc. The label includes storage instructions to protect from light and maintain controlled room temperature. The product name, strength, route, and manufacturer are prominently shown on multiple sides of the carton.*

FDA Label Image

Ndc 0641-6192-01 Rx Only 1 mL Single-dose Prefilled Syringe 462-860-00 Morphine Sulfate Injection, Usp 4 mg/ml For Iv Use Only (Morphine Sulfate Injection Usp Syringes 6)

Morphine Sulfate Injection, USP 4 mg/mL in a 1 mL single-dose prefilled syringe. The label includes NDC 0641-6192-01 and specifies Rx only. It is labeled for intravenous use and manufactured by Hikma Pharmaceuticals USA Inc.*

FDA Label Image

Ndc 0641-6192-10 Rx Only Morphine Sulfate Injection, Usp 4 mg/ml For Intravenous Use Only No Added Preservative 10 X 1 mL Single-dose Prefilled Syringes Discard Unused Portion. (Morphine Sulfate Injection Usp Syringes 7)

Packaging label for Morphine Sulfate Injection, USP 4 mg/mL by Hikma Pharmaceuticals USA Inc. This label is for single-dose 1 mL prefilled syringes for intravenous use only with no added preservative. Directions mention discarding unused portions and storage instructions between 20° to 25°C. The label displays the drug name, strength, route, dosage form, manufacturer, and usage precautions.*

* 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.