Enoxaparin Sodium Injection
Product Images NDC 16714-046

Product Visual Gallery

This gallery contains 23 technical images submitted to the FDA as part of the official labeling for Enoxaparin Sodium (NDC 16714-046). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northstar Rx Llc, 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

Eno0d 0002 01

An instructional illustration showing two hands connecting a syringe to a vial or cap, indicated by arrows pointing inward toward the connection point. This diagram likely demonstrates preparing the Enoxaparin Sodium injection for subcutaneous use.*

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Eno0d 0002 02

An instructional illustration showing a hand holding a syringe to administer a subcutaneous injection into the skin of another hand. An arrow indicates the direction of the injection into the hand's skin layer.*

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Eno0d 0002 03

An instructional illustration showing a hand injecting medication subcutaneously with a syringe. The syringe is inserted into the skin at a slight angle, indicated by an arrow pointing outward from the injection site.*

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Eno0d 0002 04

An instructional illustration showing a hand holding a syringe. An arrow points upward along the thumb, indicating the direction for thumb movement or pressure during injection preparation or administration.*

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Eno0d 0002 05

Illustration showing a hand disposing a syringe into a container labeled with a biohazard symbol, indicating safe disposal of injection needles or sharps.*

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Eno0d 0002 06

Chemical structure diagram of Enoxaparin Sodium, depicting repeating sugar units with specified R1 and R2 groups denoting hydrogen or sulfate/carbonyl-containing substituents. The structure highlights the polysaccharide nature of the active ingredient.*

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Eno0d 0002 07

Chemical structure diagram showing the molecular structure of Enoxaparin Sodium with annotations of variable groups (X*, n) and chemical groups such as COONa, OH, and NHSO3Na, indicating its complex polysaccharide format.*

FDA Label Image

Eno0d 0002 08

A forest plot chart depicting relative risk comparisons between Enoxaparin Sodium and Unfractionated Heparin (UFH) across various patient subgroups. It shows relative risk values with confidence intervals for factors including sex, age, infarct location, diabetes status, prior myocardial infarction, fibrinolytic agent type, time to treatment, and PCI within 30 days, indicating relative efficacy between Enoxaparin and UFH.*

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Eno0d 0002 09

A Kaplan-Meier hazard distribution curve comparing time to death or myocardial reinfarction over 30 days between patients treated with Enoxaparin and UFH. The chart plots hazard distribution function on the y-axis against time in days on the x-axis, showing lower hazard for Enoxaparin. A smaller inset graph extends the comparison to one year. Number of patients at risk for each group is displayed below the main chart.*

FDA Label Image

Eno0d 0002 10

Label for Enoxaparin Sodium Injection, USP, 30 mg per 0.3 mL single-dose prefilled syringe by NorthStar Rx LLC. The label includes dosage and administration information, storage instructions, and barcode with NDC 16714-006-01. The injection is for subcutaneous use.*

FDA Label Image

Eno0d 0002 11

Enoxaparin Sodium Injection, USP 30 mg per 0.3 mL subcutaneous injection carton by NorthStar Rx LLC. The packaging is for 10 single-dose prefilled syringes with an automatic safety device. The label includes usage directions, storage instructions, warnings, manufacturer information, and a barcode.*

FDA Label Image

Eno0d 0002 12

Label for Enoxaparin Sodium Injection, USP, displaying a strength of 40 mg per 0.4 mL. This is a subcutaneous injection in a single-dose prefilled syringe with a safety device. The label shows the NorthStar Rx LLC as the manufacturer and includes the NDC 16714-016-01, barcode, lot, and expiration fields, along with storage instructions and usage information.*

FDA Label Image

Eno0d 0002 13

Enoxaparin Sodium Injection USP 40 mg per 0.4 mL label for subcutaneous injection, featuring 10 x 0.4 mL single-dose prefilled syringes with automatic safety device. The label includes dosage instructions, storage information, manufacturer details (NorthStar Rx LLC), and warnings about the product being sterile and free of preservatives, PVC, and DEHP. The label design uses yellow, white, and blue colors with clear branding and a barcode.*

FDA Label Image

Eno0d 0002 14

Label for Enoxaparin Sodium Injection, USP, showing a strength of 60 mg per 0.6 mL in a single-dose prefilled syringe. The label includes dosing instructions, warnings, and manufacturer information for NorthStar Rx LLC. The image also displays the NDC number 16714-026-01 and a barcode.*

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Eno0d 0002 15

Packaging label for Enoxaparin Sodium Injection USP, 60 mg per 0.6 mL, single-dose prefilled syringes with automatic safety device. This subcutaneous injection is presented in a box containing 10 syringes of 0.6 mL each, manufactured by NorthStar Rx LLC. The label includes usage directions, storage instructions, and a barcode.*

FDA Label Image

Eno0d 0002 16

Label for Enoxaparin Sodium Injection, USP showing a strength of 80 mg per 0.8 mL. It is a single-dose subcutaneous injection packaged by NorthStar Rx LLC, with instructions and warnings printed alongside a barcode, lot, and expiration date fields. The label features a peel here tab and the NDC number 16714-036-01.*

FDA Label Image

Eno0d 0002 17

Packaging label for Enoxaparin Sodium Injection, USP 80 mg per 0.8 mL single-dose prefilled syringes with automatic safety device, for subcutaneous injection. The label indicates 10 syringes per box and notes the product is Rx only, sterile, nonpyrogenic, preservative-free, PVC-free, and DEHP-free. Manufactured for Northstar Rx LLC.*

FDA Label Image

Eno0d 0002 18

Label for Enoxaparin Sodium Injection, USP 100 mg per mL, a subcutaneous injection provided by NorthStar Rx LLC. The label indicates this is a single-dose injection with an automatic safety device and includes an NDC number 16714-046-01. It features dosage and storage information, a barcode, and batch and expiration date fields.*

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Eno0d 0002 19

Packaging label for Enoxaparin Sodium Injection USP 100 mg per mL, a subcutaneous injection supplied as 10 x 1 mL single-dose prefilled syringes with automatic safety device. The label shows usage directions, storage instructions, and warnings. It is manufactured for NorthStar Rx LLC, Memphis, TN, with manufacturing by Nanjing King-Friend Biochemical Pharmaceutical Co., China.*

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Eno0d 0002 20

Label for Enoxaparin Sodium Injection, USP, showing strength 120 mg per 0.8 mL in a single-dose prefilled syringe with a safety device. The label includes the NDC 16714-056-01, directions for subcutaneous injection, storage instructions, manufacturer NorthStar Rx LLC, and barcode. It is marked Rx only.*

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Eno0d 0002 21

Packaging label for Enoxaparin Sodium Injection USP, 120 mg per 0.8 mL, offered as 10 single-dose prefilled syringes with an automatic safety device. This subcutaneous injection is supplied by NorthStar Rx LLC. The label includes directions for use, storage instructions, and manufacturing details from Northstar Rx LLC and Nanjing King-Friend Biochemical Pharmaceutical Co., Ltd.*

FDA Label Image

Eno0d 0002 22

Label for Enoxaparin Sodium Injection, USP 150 mg per mL by NorthStar Rx LLC. This is a 1 mL single-dose prefilled syringe for subcutaneous injection. The label includes dosage information, storage instructions, manufacturer details, NDC 16714-066-01, and spaces for lot and expiration dates.*

FDA Label Image

Eno0d 0002 23

Packaging label for Enoxaparin Sodium Injection USP 150 mg per mL by NorthStar Rx LLC. The label indicates the product is a 10 x 1 mL single-dose prefilled syringe with an automatic safety device for subcutaneous injection. The label includes usage directions, storage instructions, warnings, and manufacturing details.*

* 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.