Enoxaparin Sodium Injection, Solution
Product Images NDC 11797-761

7 FDA label images from Italfarmaco Spa · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Enoxaparin Sodium (NDC 11797-761). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Italfarmaco Spa, 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

30 mg (C361399b 34e7 4807 8386 100d1383685f 01)

30 mg (C361399b 34e7 4807 8386 100d1383685f 01)
Enoxaparin Sodium Injection USP 30 mg/0.3 mL carton label for single-dose syringes with automatic safety device for subcutaneous injection. The label shows dosing strength, manufacturer Italfarmaco S.p.A., and usage route. It indicates a package contains ten 0.3 mL syringes with directions and warnings noted.*
FDA Label Image

40 mg (C361399b 34e7 4807 8386 100d1383685f 02)

40 mg (C361399b 34e7 4807 8386 100d1383685f 02)
Packaging label for Enoxaparin Sodium Injection USP 40 mg/0.4 mL, a single-dose syringe with automatic safety device for subcutaneous injection. The label shows the product name, strength, dosage form, administration route, and manufacturer Italfarmaco SpA, Italy. The package contains ten 0.4 mL syringes and includes dosing warnings, storage instructions, and directions for use illustrations.*
FDA Label Image

60 mg (C361399b 34e7 4807 8386 100d1383685f 03)

60 mg (C361399b 34e7 4807 8386 100d1383685f 03)
Enoxaparin Sodium Injection USP 60 mg/0.6 mL single-dose syringes with automatic safety device for subcutaneous injection. The carton includes ten 0.6 mL syringes. Labeler is Italfarmaco SpA, with usage directions and storage instructions visible. The packaging features safety and dosage information alongside manufacturer details.*
FDA Label Image

80 mg (C361399b 34e7 4807 8386 100d1383685f 04)

80 mg (C361399b 34e7 4807 8386 100d1383685f 04)
Packaging label for Enoxaparin Sodium Injection USP, 80 mg/0.8 mL, a single-dose syringe with an automatic safety device for subcutaneous injection. The label includes dosage and administration instructions, storage conditions, manufacturer Italfarmaco SpA, and Zydus Pharmaceuticals branding. The package contains ten 0.8 mL syringes and is marked Rx only.*
FDA Label Image

100 mg (C361399b 34e7 4807 8386 100d1383685f 05)

100 mg (C361399b 34e7 4807 8386 100d1383685f 05)
Packaging label for Enoxaparin Sodium Injection USP 100 mg/mL in single-dose syringes with automatic safety device for subcutaneous injection. The label shows dosage form as injection solution, each syringe containing 100 mg enoxaparin sodium. The labeler is Italfarmaco SpA, Milano, Italy, and the package contains ten 1 mL syringes. Instructions for use of the syringe with safety device are also included on the label.*
FDA Label Image

120 mg (C361399b 34e7 4807 8386 100d1383685f 06)

120 mg (C361399b 34e7 4807 8386 100d1383685f 06)
Enoxaparin Sodium Injection USP 120 mg/0.8 mL packaging label for single-dose syringes with automatic safety device for subcutaneous injection. The label shows dose strength and administration route, manufacturer Italfarmaco SpA, lot of ten 0.8 mL syringes, and usage directions with illustrations. The label identifies storage instructions and warnings including Rx only status.*
FDA Label Image

150 mg (C361399b 34e7 4807 8386 100d1383685f 07)

150 mg (C361399b 34e7 4807 8386 100d1383685f 07)
Label for Enoxaparin Sodium Injection USP 150 mg/mL, a single-dose syringe with automatic safety device for subcutaneous injection. The label shows dosage form as 1 mL syringes, ten per package. Manufacturer listed is Italfarmaco SpA, with storage instructions and warnings included. The label also features illustrated instructions for use.*

* 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.