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NDC 16571-0843-50 POTASSIUM CHLORIDE EXTENDED RELEASE 750 mg/1 Details

POTASSIUM CHLORIDE EXTENDED RELEASE 750 mg/1

POTASSIUM CHLORIDE EXTENDED RELEASE is a ORAL TABLET, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Rising Pharma Holdings, Inc.. The primary component is POTASSIUM CHLORIDE.

MedlinePlus Drug Summary

Potassium is essential for the proper functioning of the heart, kidneys, muscles, nerves, and digestive system. Usually the food you eat supplies all of the potassium you need. However, certain diseases (e.g., kidney disease and gastrointestinal disease with vomiting and diarrhea) and drugs, especially diuretics ('water pills'), remove potassium from the body. Potassium supplements are taken to replace potassium losses and prevent potassium deficiency. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.

Related Packages: 16571-0843-50
Last Updated: 03/24/2024
MedLinePlus Full Drug Details: Potassium

Product Information

NDC	16571-0843
Product ID	16571-843_fe4e9cca-4035-4f2a-8802-ce569e2af05e
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	POTASSIUM CHLORIDE EXTENDED RELEASE
Proprietary Name Suffix	n/a
Non-Proprietary Name	potassium chloride
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, EXTENDED RELEASE
Route	ORAL
Active Ingredient Strength	750
Active Ingredient Units	mg/1
Substance Name	POTASSIUM CHLORIDE
Labeler Name	Rising Pharma Holdings, Inc.
Pharmaceutical Class	Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA217412
Listing Certified Through	2024-12-31

Package

NDC 16571-0843-50 (16571084350)

Pricing Information	N/A
NDC Package Code	16571-843-50
Billing NDC	16571084350
Package	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (16571-843-50)
Marketing Start Date	2023-12-19
NDC Exclude Flag	N