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, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 750 mg/1

Manufacturer
Aphena Pharma Solutions - Tennessee, LLC

Identifiers & Regulatory

Product NDC 71610-944
Product ID 71610-944_3dfa6220-3a05-7ca6-e063-6394a90ac879
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210921
Listing Expiration 2026-12-31
Marketing Start 2018-12-19

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 71610944
Hyphenated Format 71610-944

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 ANDA210921 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-944-30)
  • 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-944-53)
  • 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-944-60)
  • 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-944-70)
source: ndc

Packages (4)

Ingredients (1)

potassium chloride (750 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3dfa6220-3a05-7ca6-e063-6394a90ac879", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["628953"], "spl_set_id": ["3dfa63fc-f8de-f1e0-e063-6294a90a8d47"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-944-30)", "package_ndc": "71610-944-30", "marketing_start_date": "20250903"}, {"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-944-53)", "package_ndc": "71610-944-53", "marketing_start_date": "20250903"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-944-60)", "package_ndc": "71610-944-60", "marketing_start_date": "20250903"}, {"sample": false, "description": "120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-944-70)", "package_ndc": "71610-944-70", "marketing_start_date": "20250903"}], "brand_name": "Potassium Chloride", "product_id": "71610-944_3dfa6220-3a05-7ca6-e063-6394a90ac879", "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": "71610-944", "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": "ANDA210921", "marketing_category": "ANDA", "marketing_start_date": "20181219", "listing_expiration_date": "20261231"}