potassium chloride

Generic: potassium chloride

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

Drug Facts

Product Profile

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

potassium chloride 1500 mg/1

Manufacturer
Aphena Pharma Solutions - Tennessee, LLC

Identifiers & Regulatory

Product NDC 71610-343
Product ID 71610-343_142e9197-d146-48fa-9b27-86cced0fbfba
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074726
Listing Expiration 2026-12-31
Marketing Start 2019-06-19

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 71610343
Hyphenated Format 71610-343

Supplemental Identifiers

RxCUI
1801294
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 ANDA074726 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1500 mg/1
source: ndc
Packaging
  • 15 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-343-15)
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-343-30)
  • 45 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-343-45)
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-343-53)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-343-60)
  • 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-343-70)
  • 135 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-343-73)
  • 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-343-80)
  • 240 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-343-90)
  • 270 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-343-92)
source: ndc

Packages (10)

71610-343-15 15 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-343-15) 71610-343-30 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-343-30) 71610-343-45 45 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-343-45) 71610-343-53 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-343-53) 71610-343-60 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-343-60) 71610-343-70 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-343-70) 71610-343-73 135 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-343-73) 71610-343-80 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-343-80) 71610-343-90 240 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-343-90) 71610-343-92 270 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-343-92)

Ingredients (1)

potassium chloride (1500 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": "142e9197-d146-48fa-9b27-86cced0fbfba", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1801294"], "spl_set_id": ["d2e84d34-e042-477f-9944-3fcb95301217"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-343-15)", "package_ndc": "71610-343-15", "marketing_start_date": "20191101"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-343-30)", "package_ndc": "71610-343-30", "marketing_start_date": "20190918"}, {"sample": false, "description": "45 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-343-45)", "package_ndc": "71610-343-45", "marketing_start_date": "20190918"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-343-53)", "package_ndc": "71610-343-53", "marketing_start_date": "20190918"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-343-60)", "package_ndc": "71610-343-60", "marketing_start_date": "20190918"}, {"sample": false, "description": "120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-343-70)", "package_ndc": "71610-343-70", "marketing_start_date": "20220224"}, {"sample": false, "description": "135 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-343-73)", "package_ndc": "71610-343-73", "marketing_start_date": "20191025"}, {"sample": false, "description": "180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-343-80)", "package_ndc": "71610-343-80", "marketing_start_date": "20190918"}, {"sample": false, "description": "240 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-343-90)", "package_ndc": "71610-343-90", "marketing_start_date": "20201009"}, {"sample": false, "description": "270 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-343-92)", "package_ndc": "71610-343-92", "marketing_start_date": "20190918"}], "brand_name": "Potassium Chloride", "product_id": "71610-343_142e9197-d146-48fa-9b27-86cced0fbfba", "dosage_form": "TABLET, 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": "71610-343", "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": "1500 mg/1"}], "application_number": "ANDA074726", "marketing_category": "ANDA", "marketing_start_date": "20190619", "listing_expiration_date": "20261231"}