potassium chloride

Generic: potassium chloride

Labeler: aphena pharma solutions - tennessee, llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler aphena pharma solutions - tennessee, llc
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 750 mg/1

Manufacturer
Aphena Pharma Solutions - Tennessee, LLC

Identifiers & Regulatory

Product NDC 71610-349
Product ID 71610-349_2b497b8f-a0e3-9ff7-e063-6394a90a3800
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA019123
Listing Expiration 2026-12-31
Marketing Start 2019-06-21

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 71610349
Hyphenated Format 71610-349

Supplemental Identifiers

RxCUI
628953
UNII
660YQ98I10

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 NDA019123 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 15 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-15)
  • 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-30)
  • 45 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-45)
  • 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-53)
  • 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-60)
  • 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-70)
  • 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-80)
  • 200 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-85)
  • 270 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-92)
  • 360 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-94)
  • 540 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-98)
source: ndc

Packages (11)

71610-349-15 15 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-15) 71610-349-30 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-30) 71610-349-45 45 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-45) 71610-349-53 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-53) 71610-349-60 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-60) 71610-349-70 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-70) 71610-349-80 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-80) 71610-349-85 200 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-85) 71610-349-92 270 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-92) 71610-349-94 360 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-94) 71610-349-98 540 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-98)

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": "2b497b8f-a0e3-9ff7-e063-6394a90a3800", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["628953"], "spl_set_id": ["81a53ecd-2612-4efe-9491-415fff3f86e5"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-15)", "package_ndc": "71610-349-15", "marketing_start_date": "20220208"}, {"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-30)", "package_ndc": "71610-349-30", "marketing_start_date": "20191016"}, {"sample": false, "description": "45 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-45)", "package_ndc": "71610-349-45", "marketing_start_date": "20220208"}, {"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-53)", "package_ndc": "71610-349-53", "marketing_start_date": "20191016"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-60)", "package_ndc": "71610-349-60", "marketing_start_date": "20191016"}, {"sample": false, "description": "120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-70)", "package_ndc": "71610-349-70", "marketing_start_date": "20191016"}, {"sample": false, "description": "180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-80)", "package_ndc": "71610-349-80", "marketing_start_date": "20191016"}, {"sample": false, "description": "200 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-85)", "package_ndc": "71610-349-85", "marketing_start_date": "20191016"}, {"sample": false, "description": "270 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-92)", "package_ndc": "71610-349-92", "marketing_start_date": "20191016"}, {"sample": false, "description": "360 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-94)", "package_ndc": "71610-349-94", "marketing_start_date": "20191016"}, {"sample": false, "description": "540 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-349-98)", "package_ndc": "71610-349-98", "marketing_start_date": "20220208"}], "brand_name": "Potassium Chloride", "product_id": "71610-349_2b497b8f-a0e3-9ff7-e063-6394a90a3800", "dosage_form": "TABLET, FILM COATED, 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": "71610-349", "generic_name": "Potassium Chloride", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "NDA019123", "marketing_category": "NDA", "marketing_start_date": "20190621", "listing_expiration_date": "20261231"}