70518-1188 : Potassium Chloride 1500 mg Oral Tablet, Film Coated, Extended Release

NDC:	70518-1188
Labeler:	Remedyrepack Inc.
Product Type:	Human Prescription Drug
Drug Name:	Potassium Chloride
Dosage Form:	Oral Tablet, Film Coated, Extended Release
Application #:	NDA018279
Rev. Date:	May 14, 2018

Appearance:

Markings:	KTAB
Shapes:	Oval
Colors:	White
Size (mm):	20
Segments: ^*	1
^* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines.

NDC Package Codes:

70518-1188-0: 60 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE, PLASTIC (70518‑1188‑0)

Active Ingredients:

Potassium Chloride

Dosage Strength:

1500 mg

Inactive Ingredients:

Castor Oil
Silicon Dioxide
Magnesium Stearate
Paraffin
Titanium Dioxide
Vanillin
.alpha.-tocopherol
Polyvinyl Acetate
Ethylcellulose, Unspecified /

Pharmaceutical Classes:

Potassium Compounds [CS]
Potassium Salt [EPC]
Osmotic Laxative [EPC]
Increased Large Intestinal Motility [PE]
Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]
Osmotic Activity [MoA]

NDC QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.