Potassium Chloride
Product Images NDC 60219-1069

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Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Potassium Chloride (NDC 60219-1069). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals Ny 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

10 Meq K (Potassium Chloride Extended Release Tablets Usp 1)

10 Meq K (Potassium Chloride Extended Release Tablets Usp 1)
Each extended-release tablet of NDC 60219-1065-1 contains 750 mg of potassium chloride, USP, which is equivalent to 10 mEq of potassium. Dosage must be individualized for each patient. Refer to the accompanying package insert for full prescribing information and visual dosage. Store the tablets at 20° to 25°C (68° to 77°F) and keep them tightly closed in a tight, light-resistant container as defined in the USP. Excursions between 15° to 30°C (50° to 86°F) are permitted. Amneal Pharmaceuticals Ltd. manufactures the tablets in Ahmedabad, India, and Amneal Pharmaceuticals LLC distributes them in Bridgewater, NJ. The FDA's approved criteria for assay may differ from the USP test. Keep the tablets out of children's reach.*
FDA Label Image

15 Meq K (Potassium Chloride Extended Release Tablets Usp 2)

15 Meq K (Potassium Chloride Extended Release Tablets Usp 2)
Each tablet of this medication (NDC 60219-1065-7) contains 750mg of potassium chloride, which is equivalent to 10 milliequivalents of potassium. The dosage of the extended-release medication should be customized according to the individual needs of each patient, and the full prescribing information is available in the package insert. The tablets should be stored at a temperature between 20 to 25°C (68° to 77°F), with excursions permitted between 15° to 30°C (59° to 86°F). The medication must be kept tightly closed and in a tight, light-resistant container, out of reach of children. The FDA approved assay criteria for this medication are different from the USP test. The medication is manufactured by Amneal Pharmaceuticals Pvt. Ltd. in India and distributed by Amneal Pharmaceuticals LLC in Bridgewater, NJ.*
FDA Label Image

20 Meq K (Potassium Chloride Extended Release Tablets Usp 3)

FDA Label Image

Potassium Chloride Extended Release Tablets Usp 4

Potassium Chloride Extended Release Tablets Usp 4
This is a description of Potassium Chloride Extended-Release Tablets, USP with a strength of 1,500 mg/tablet (equivalent to 20 mEq of potassium). The dosage must be tailored to individual needs, and storage must be at 20-25°C (68-77°F) with tight closure and protection from light. The tablets should be dispensed in a tight, light-resistant container and kept out of the reach of children. These tablets are manufactured by Amneal Pharmaceuticals Pvt. Ltd. in India and distributed by Amneal Pharmaceuticals LLC in Bridgewater, NJ. The FDA has approved these tablets with different acceptance criteria for assay compared to the USP test.*
FDA Label Image

Potassium Chloride Extended Release Tablets Usp 5

Potassium Chloride Extended Release Tablets Usp 5
This is a potassium chloride extended-release tablet. Each tablet contains 1,500 mg of potassium chloride (equivalent to 20 mEq of potassium) and must be adjusted according to the individual needs of each patient. The recommended dosage is included in the package insert. The tablets should be stored at room temperature and in a tightly closed container. The manufacturer is Amneal Pharmaceuticals Pvt. Ltd, located in Ahmedabad, India, and the product is distributed by Amneal Pharmaceuticals LLC located in Bridgewater, NJ.*

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