Potassium Chloride For Solution
Product Images NDC 43386-194

3 FDA label images from Lupin Pharmaceuticals,inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Potassium Chloride (NDC 43386-194). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lupin Pharmaceuticals,inc., 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

Pouch (44a9f91b 6278 4ae2 Bcdd Fee8ce50e9da 01)

Pouch (44a9f91b 6278 4ae2 Bcdd Fee8ce50e9da 01)
Potassium Chloride for Oral Solution, USP, 20 mEq strength, in single-dose 1.5 g packaging, labeled by Lupin Pharmaceuticals, Inc. The label indicates prescription use only.*
FDA Label Image

Carton-30 Ct (44a9f91b 6278 4ae2 Bcdd Fee8ce50e9da 02)

Carton-30 Ct (44a9f91b 6278 4ae2 Bcdd Fee8ce50e9da 02)
Potassium Chloride for Oral Solution, USP 20 mEq in 1.5 g single-dose pouches, orange flavored. The carton contains 30 single-dose pouches. Labeler is Lupin Pharmaceuticals, Inc. The packaging includes dosage instructions, storage information, and manufacturer details from Novel Laboratories, Inc. and Lupin Pharmaceuticals, Inc.*
FDA Label Image

Carton-100 Ct (44a9f91b 6278 4ae2 Bcdd Fee8ce50e9da 03)

Carton-100 Ct (44a9f91b 6278 4ae2 Bcdd Fee8ce50e9da 03)
Potassium Chloride for Oral Solution, USP 20 mEq (1.5 g) in single-dose pouches, 100 count carton. Oral solution form, orange flavored, manufactured for Lupin Pharmaceuticals, Inc., labeled as Rx only. Directions note dissolving one pouch in 4 ounces of water or beverage. Produced by Novel Laboratories, Inc., Somerset, NJ.*

* 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.