Octreotide Acetate Injection, Solution
Product Images NDC 0641-6174

8 FDA label images from Hikma Pharmaceuticals Usa Inc. · 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 Octreotide Acetate (NDC 0641-6174). 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 (Octreotide Acetate Injection 1)

Chemical Structure (Octreotide Acetate Injection 1)
Chemical structure diagram of Octreotide Acetate displaying its peptide sequence with amino acid abbreviations and notation indicating the variable component 'x' in the formula.*
FDA Label Image

West-ward Logo (Octreotide Acetate Injection 2)

West-ward Logo (Octreotide Acetate Injection 2)
Octreotide Acetate Injection 50 mcg/mL label from Hikma Pharmaceuticals USA Inc. The label indicates a 1 mL single-dose vial for subcutaneous injection, storage at 2° to 8°C, and shows the NDC 0641-6174-01. Additional fields for lot and expiration date are present but not filled.*
FDA Label Image

50 Mcg/ml Container Label (Octreotide Acetate Injection 3)

50 Mcg/ml Container Label (Octreotide Acetate Injection 3)
Label for Octreotide Acetate Injection 100 mcg/mL by Hikma Pharmaceuticals USA Inc. The label indicates the product is for subcutaneous injection, stored at 2° to 8°C, and comes as a 1 mL single dose vial. Includes NDC number 0641-6175-01 and barcode with lot and expiration date fields.*
FDA Label Image

462-720-01 (Octreotide Acetate Injection 4)

462-720-01 (Octreotide Acetate Injection 4)
Label for Octreotide Acetate Injection 500 mcg/mL solution for injection. It is intended for subcutaneous use and comes in a 1 mL single dose vial. The label includes storage instructions (2° to 8°C) and is manufactured by Hikma Pharmaceuticals USA Inc. NDC 00641-6176-01 is visible.*
FDA Label Image

100 Mcg/ml Container Label (Octreotide Acetate Injection 5)

100 Mcg/ml Container Label (Octreotide Acetate Injection 5)
Label for Octreotide Acetate Injection 1,000 mcg per 5 mL (200 mcg/mL) by Hikma Pharmaceuticals USA Inc. It is a 5 mL multiple dose vial intended for subcutaneous injection. The label includes storage instructions (refrigerate at 2 to 8°C, protect from light) and disposal guidance (discard within 14 days after first use).*
FDA Label Image

462-722-01 (Octreotide Acetate Injection 6)

462-722-01 (Octreotide Acetate Injection 6)
Label for Octreotide Acetate Injection 5,000 mcg per 5 mL (1,000 mcg/mL) for subcutaneous injection, provided as a 5 mL multiple dose vial. The product is labeled for prescription use only and manufactured by Hikma Pharmaceuticals USA Inc. Storage instructions indicate refrigeration and protection from light.*
FDA Label Image

500 Mcg/mlcontainer Label (Octreotide Acetate Injection 7)

500 Mcg/mlcontainer Label (Octreotide Acetate Injection 7)
QR code label showing product identification data including GTIN, serial number, expiration date placeholder, and lot number. The label does not specify drug name or strength but contains typical traceability information for Octreotide Acetate injection by Hikma Pharmaceuticals USA Inc.*
FDA Label Image

462-724-01 (Octreotide Acetate Injection 8)

462-724-01 (Octreotide Acetate Injection 8)
A label featuring a QR code and identifying information typical for pharmaceutical products. It includes lot number ABCDE12345, an expiration date placeholder (MMMYYYY), a GTIN barcode number 00301234567896, and a serial number 12345678901234. No brand or dosage details are visible beyond this barcode data.*

* 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.