Potassium Chloride

Product NDC: 51655-587
11-digit product format: 516550587
Labeler code: 51655
Product ID: 51655-587_7189242f-370a-43ea-b08d-a962eb89d6da
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Potassium Chloride ER
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Route: ORAL
Labeler: Northwind Pharmaceuticals
Application: NDA018279
Marketing category: NDA
Marketing start: 2014-01-21
Marketing end: 0000-00-00
Substance: POTASSIUM CHLORIDE
Active strength: 750 mg/1
Pharmacologic 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 exclude flag: No
Listing certified through: 2019-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
51655-587-52	2026-01-08	C162847	48780-1	9d75b9cf-d688-f424-e053-dadaa90a57ce	3aef07da-ca04-4fa4-a0ea-e84ee3fef555
51655-587-52	2020-01-31	C162847	48780-1	9d75b9cf-d688-f424-e053-dadaa90a57ce	3aef07da-ca04-4fa4-a0ea-e84ee3fef555

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
POTASSIUM CHLORIDE	ACTIVE INGREDIENT	660YQ98I10	POTASSIUM CHLORIDE ER TABLET, FILM COATED, EXTENDED RELEASE [NORTHWIND PHARMACEUTICALS]	1
POTASSIUM CATION	ACTIVE MOIETY	295O53K152	POTASSIUM CHLORIDE ER TABLET, FILM COATED, EXTENDED RELEASE [NORTHWIND PHARMACEUTICALS]	1

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51655-587	POTASSIUM CHLORIDE ER TABLET, FILM COATED, EXTENDED RELEASE [NORTHWIND PHARMACEUTICALS]	1	Legacy NDC	20150122_3aef07da-ca04-4fa4-a0ea-e84ee3fef555.zip