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NDC 71335-1747-01 Potassium Chloride 1500 mg/1 Details

Potassium Chloride 1500 mg/1

Potassium Chloride is a ORAL TABLET, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. 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: 71335-1747-01
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Potassium

Product Information

NDC	71335-1747
Product ID	71335-1747_fdf3e671-7d42-cca8-e053-6294a90a277e
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
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	1500
Active Ingredient Units	mg/1
Substance Name	POTASSIUM CHLORIDE
Labeler Name	Bryant Ranch Prepack
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	ANDA074726
Listing Certified Through	2024-12-31

Package

NDC 71335-1747-01 (71335174701)

Pricing Information	N/A
NDC Package Code	71335-1747-1
Billing NDC	71335174701
Package	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1747-1)
Marketing Start Date	2020-12-17
NDC Exclude Flag	N