68382-776 : Potassium Chloride 600 mg Oral Tablet, Film Coated, Extended Release

NDC:	68382-776
Labeler:	Zydus Pharmaceuticals USA Inc
Product Type:	Human Prescription Drug
Drug Name:	Potassium Chloride
Dosage Form:	Oral Tablet, Film Coated, Extended Release
Application #:	NDA018279
Rev. Date:	Jan 16, 2014

Appearance:

Markings:	KTAB
Shapes:	Round
Colors:	Yellow
Size (mm):	11
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.

KTAB: (68382-776) Potassium Chloride 600 mg Oral Tablet, Film Coated, Extended Release by Zydus Pharmaceuticals USA Inc

The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.

NDC Package Codes:

68382-776-01: 100 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE (68382‑776‑01)
68382-776-10: 1000 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE (68382‑776‑10)

Active Ingredients:

Potassium Chloride

Dosage Strength:

600 mg

Inactive Ingredients:

Castor Oil
Silicon Dioxide
Magnesium Stearate
Paraffin
Titanium Dioxide
Vanillin
Ethylcelluloses
.alpha.-tocopherol
Polyvinyl Acetate
D&c Yellow No. 10

Pharmaceutical Classes:

Potassium Compounds [Chemical/Ingredient]
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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NDC 68382-776 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.