potassium chloride

Generic: potassium chloride

Labeler: actavis pharma, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler actavis pharma, inc.
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 750 mg/1

Manufacturer
Actavis Pharma, Inc.

Identifiers & Regulatory

Product NDC 62037-560
Product ID 62037-560_57df625b-891f-4826-a64b-46db5e64378e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077419
Marketing Start 2008-08-25
Marketing End 2026-10-31

Pharmacologic Class

Classes
increased large intestinal motility [pe] inhibition large intestine fluid/electrolyte absorption [pe] osmotic activity [moa] osmotic laxative [epc] potassium compounds [cs] potassium salt [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62037560
Hyphenated Format 62037-560

Supplemental Identifiers

RxCUI
312504 315183
UPC
0362037560903
UNII
660YQ98I10

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name potassium chloride (source: ndc)
Generic Name potassium chloride (source: ndc)
Application Number ANDA077419 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-560-01)
  • 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-560-05)
  • 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-560-10)
  • 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-560-90)
source: ndc

Packages (4)

62037-560-01 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-560-01) 62037-560-05 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-560-05) 62037-560-10 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-560-10) 62037-560-90 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-560-90)

Ingredients (1)

potassium chloride (750 mg/1)

Linked Drug Pages (1)

Potassium Chloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "57df625b-891f-4826-a64b-46db5e64378e", "openfda": {"upc": ["0362037560903"], "unii": ["660YQ98I10"], "rxcui": ["312504", "315183"], "spl_set_id": ["ed5baaf6-270b-4dd3-b100-36030c0098fc"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-560-01)", "package_ndc": "62037-560-01", "marketing_end_date": "20261031", "marketing_start_date": "20080825"}, {"sample": false, "description": "500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-560-05)", "package_ndc": "62037-560-05", "marketing_end_date": "20261031", "marketing_start_date": "20080825"}, {"sample": false, "description": "1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-560-10)", "package_ndc": "62037-560-10", "marketing_end_date": "20261031", "marketing_start_date": "20080825"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-560-90)", "package_ndc": "62037-560-90", "marketing_end_date": "20260531", "marketing_start_date": "20080825"}], "brand_name": "Potassium Chloride", "product_id": "62037-560_57df625b-891f-4826-a64b-46db5e64378e", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_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]"], "product_ndc": "62037-560", "generic_name": "Potassium Chloride", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA077419", "marketing_category": "ANDA", "marketing_end_date": "20261031", "marketing_start_date": "20080825"}