Calcium Gluconate Injection
Product Images NDC 80830-1672

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Calcium Gluconate (NDC 80830-1672). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals Private Limited, 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

1 (Calcium Gluconate Injection 100 mg Per mL 1)

FDA Label Image

8 (Calcium Gluconate Injection 100 mg Per mL 10)

FDA Label Image

1 (Calcium Gluconate Injection 100 mg Per mL 2)

This is a product description for Calcium Gluconate Injection, USP. It is a preservative-free solution intended for intravenous use. The product comes in a 10 mL single-dose vial with the National Drug Code (NDC) 80830-1672.*

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5 (Calcium Gluconate Injection 100 mg Per mL 3)

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4 (Calcium Gluconate Injection 100 mg Per mL 4)

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2 (Calcium Gluconate Injection 100 mg Per mL 5)

This text contains information about Calcium Gluconate Injection, USP, specifically designed for intravenous use. The product is available in a preservative-free 50 mL single-dose vial with NDC 80830-1673-1. The text may also contain some codes or identifiers for the product.*

FDA Label Image

7 (Calcium Gluconate Injection 100 mg Per mL 6)

This is a product description for Calcium Gluconate Injection, USP, with a concentration of 5,000 mg per 50 mL. It is intended for intravenous use only and comes in 10 x 50 mL single-dose vials. The solution is preservative-free and must be stored at 20° to 25°C. Instructions for reconstitution are provided for bolus intravenous administration and continuous intravenous infusion. It is important not to mix calcium gluconate injection with certain other drugs. The text also includes manufacturing and distribution details.*

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6 (Calcium Gluconate Injection 100 mg Per mL 7)

This text provides information about Calcium Gluconate Injection, USP, with details on dosage, reconstitution instructions, storage conditions, and precautions. It mentions the contents of each mL, the presence of preservatives, and emphasizes that the solution should be used only if clear and the seal is intact. It also includes instructions for both bolus intravenous administration and continuous intravenous infusion. The text warns against mixing Calcium Gluconate Injection with certain medications and highlights that the diluted solution must be used immediately.*

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3 (Calcium Gluconate Injection 100 mg Per mL 8)

This text is a detailed description of a Pharmacy Bulk Package containing sterile calcium gluconate solution with specific concentrations and instructions for use. It is intended for pharmacy admixture programs and must be dispensed within 4 hours after the container closure is penetrated. The solution should be stored at room temperature, and precautions are mentioned to prevent precipitation of supersaturated solutions. The package is free from natural rubber latex and contains no more than 400 mcg/L of aluminum. The text also provides information on the manufacturer and distributor of the product.*

FDA Label Image

9 (Calcium Gluconate Injection 100 mg Per mL 9)

This is a detailed description of a pharmaceutical product. It is a bulk package of Calcium Gluconate Injection, USP, containing 410,000 mg per 100 mL (100 mg per mL) for intravenous use only. The package includes 10 x 100 mL vials that are preservative-free. The text also mentions the contents of schard, mosmolnt, and instructions for proper storage and administration of the solution.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.