Potassium Chloride
Product Images NDC 67296-1814

View Photos of 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 67296-1814). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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

Epm 6 Count (67296 1814 6)

Epm 6 Count (67296 1814 6)
This is a description of a prescription medication bottle containing Potassium Chloride Extended Release capsules, with a strength of 10mEq (750mg) and a total of 6 capsules per bottle. The bottle is labeled with an expiration date of 02/23 and a lot number of 000934X1. The usual adult dosage and storage instructions are contained within the package insert. The medication is distributed by Redpharm Drug and the manufacturer is Mig Lupin Limited located in Pithampur, India. The NDC number is 67296-1814-6, and the bottle also bears the codes 68180-799-01 and 67296 18146 3. The text includes seemingly random numbers and symbols that may not be relevant to the prescription medication.*
FDA Label Image

Imgae-01 (F8b0abaa A436 43f5 9381 F3cf011bcd17 01)

Imgae-01 (F8b0abaa A436 43f5 9381 F3cf011bcd17 01)
NDC 68180-798-01 is the code for Potassium Chloride Extended-Release Capsules containing microencapsulated KCland, manufactured by Lupin Pharmaceuticals, Inc. The capsules are designed to release the active ingredient over an 8-to-10-hour period and the recommended USP dosage is to be followed as detailed in the accompanying prescribing information. The capsules must be stored in a tightly closed container at 25°C (77°F); excursions permitted 15 to 30°C (59 to 86°F) [See USP) Controlled Room Temperature]. Each container dispenses 600 mg capsules. The manufacturer of this product is Lupin Limited, and the manufacturing site is located in Pithampur (M.P) 454 775, INDIA.*
FDA Label Image

Image 02 (F8b0abaa A436 43f5 9381 F3cf011bcd17 02)

Image 02 (F8b0abaa A436 43f5 9381 F3cf011bcd17 02)
NDC 68180-799-01 is a medication containing 10 mEq of microencapsulated potassium chloride. It is designed to release the active ingredient over an 8-to-10-hour period. The usual dosage should be taken after referring to the accompanying prescribing information. It should be stored at 25°C (77°F). Lupin Pharmaceuticals, Inc. manufacture the medication, while Lupin Limited manufactures the extended-release capsules USP. It must be tightly stored in a container as defined by the USP. 100 capsules of this medication can be dispensed per pack.*

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