Product Images Potassium Chloride

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Product Label Images

The following 3 images provide visual information about the product associated with Potassium Chloride NDC 67296-1771 by Redpharm Drug, Inc., such as packaging, labeling, and the appearance of the drug itself. This resource could be helpful for medical professionals, pharmacists, and patients seeking to verify medication information and ensure they have the correct product.

LABEL - 67296 1771

LABEL - 67296 1771

This is a description of a medication called Potassium Chloride ER, which comes in the form of 30 tablets. It has a strength of 10mEq (750MG) and requires a prescription. The medication is stored at controlled room temperature (20-25 C / 68-77 F) and should be used according to the instructions contained within the package insert. The manufacturing company is Mig Strides Shasun Ltd in India, and it is distributed by Redpharm Drug in Eden Prairie, Minnesota. The Lot number is 38256AX1, with an expiration date of 06/21. The National Drug Code is 67296-1771-3.*

600mg - 853af0b0 dc2a 46ce 9ca2 89dc07cae63d 01

600mg - 853af0b0 dc2a 46ce 9ca2 89dc07cae63d 01

This is a prescription drug called Potassium Chloride USP in extended-release tablet form. The usual dose information is provided in the accompanying package insert, and dosage must be adjusted according to individual patient needs. It should be stored at 25°C, protected from light and moisture, and dispensed in a tight container with a child-resistant closure. Patients are advised that the expended matrix may pass through the digestive system without being absorbed. The drug is distributed by Strides Pharma Inc. and FDA approved, with batch details provided on the packaging.*

750mg - 853af0b0 dc2a 46ce 9ca2 89dc07cae63d 02

750mg - 853af0b0 dc2a 46ce 9ca2 89dc07cae63d 02

This is a prescription drug, manufactured by Strides Pharma Science Limited in India and distributed by Strides Pharma Inc in East Brunswick, NJ. It is a bottle of 100 tablets of Potassium Chloride USP, Extended-Release. Each tablet contains 750mg of the active ingredient. It is important to adjust the dosage to the individual needs of each patient. The drug should be stored at 25°C, in a tight container, and protected from light and moisture. The product packaging contains information on dosing, storage and other patient information. The drug was revised in December 2019. The label contains the National Drug Code (NDC) of 64380-861-06, and a caution that it contains FD&C Yellow No. 5 as a color additive. The label also indicates that the FDA approved acceptance criteria for assay differs from the USP test. The space for batch details is expected to be marked with information related to the batch number, Varnish Zone, LOT #, and expiration date.*

* The product label images have been analyzed using a combination of traditional computing and machine learning techniques. It should be noted that the descriptions provided may not be entirely accurate as they are experimental in nature. Use the information in this page at your own discretion and risk.