Calcium Gluconate Injection, Solution
Product Images NDC 80830-2363

View Photos of 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 Calcium Gluconate (NDC 80830-2363). 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 In Sodium Chloride Injection 1)

1 (Calcium Gluconate In Sodium Chloride Injection 1)
Chemical structure of calcium gluconate showing the calcium ion complexed with two gluconate molecules, including hydroxyl groups and carboxylate ions, with water (H2O) indicated.*
FDA Label Image

1 (Calcium Gluconate In Sodium Chloride Injection 2)

1 (Calcium Gluconate In Sodium Chloride Injection 2)
Label for Calcium Gluconate in Sodium Chloride Injection, 20 mg/mL (1,000 mg per 50 mL), 1 gram total. Designed for intravenous use, single-dose container with instructions not to dilute. Manufactured by Puniska Healthcare Pvt. Ltd., a subsidiary of Amneal Pharmaceuticals Pvt. Ltd., and distributed by Amneal Pharmaceuticals LLC.*
FDA Label Image

1 (Calcium Gluconate In Sodium Chloride Injection 3)

1 (Calcium Gluconate In Sodium Chloride Injection 3)
Label for Calcium Gluconate in Sodium Chloride Injection, 1,000 mg per 50 mL (20 mg/mL), for intravenous use. The single-dose container is marked as 1 g total, with manufacturer information for Puniska Healthcare Pvt. Ltd. and distributor Amneal Pharmaceuticals LLC. Storage instructions and usage precautions are provided.*
FDA Label Image

1 (Calcium Gluconate In Sodium Chloride Injection 4)

1 (Calcium Gluconate In Sodium Chloride Injection 4)
Packaging label for Calcium Gluconate in Sodium Chloride Injection, solution for intravenous use, 20 mg/mL strength. The label indicates a total of 1,000 mg per 50 mL in single-dose containers, with a package size of 24 x 50 mL. Manufactured by Puniska Healthcare Pvt. Ltd., a subsidiary of Amneal Pharmaceuticals Pvt. Ltd., and distributed by Amneal Pharmaceuticals LLC. The label includes usage instructions, storage conditions, and regulatory details.*
FDA Label Image

1 (Calcium Gluconate In Sodium Chloride Injection 5)

1 (Calcium Gluconate In Sodium Chloride Injection 5)
Calcium Gluconate in Sodium Chloride Injection label showing 2,000 mg per 100 mL (20 mg per mL) concentration. The label indicates the product is for intravenous use only and is a single-dose container. It includes manufacturer information for Puniska Healthcare Pvt. Ltd. and distributor Amneal Pharmaceuticals LLC. Dosage/storage instructions and drug components are also detailed.*
FDA Label Image

1 (Calcium Gluconate In Sodium Chloride Injection 6)

1 (Calcium Gluconate In Sodium Chloride Injection 6)
Label for Calcium Gluconate in Sodium Chloride Injection, 20 mg/mL (2000 mg per 100 mL), totaling 2 g. It is a single-dose intravenous injection solution labeled for Rx only. Manufactured by Puniska Healthcare Pvt. Ltd., distributed by Amneal Pharmaceuticals LLC. The label includes usage instructions, storage conditions, and a barcode.*
FDA Label Image

1 (Calcium Gluconate In Sodium Chloride Injection 7)

1 (Calcium Gluconate In Sodium Chloride Injection 7)
Label for Calcium Gluconate in Sodium Chloride Injection, 20 mg/mL, in 100 mL single-dose containers with 24 units per package. Manufactured by Puniska Healthcare Pvt. Ltd. and distributed by Amneal Pharmaceuticals LLC. Contains storage and usage instructions along with active ingredient details and barcode.*

* 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.