potassium chloride (71610-945)

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 71610-945

Product ID 71610-945_3dfac7d8-fe2d-eb9d-e063-6394a90a477a

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA209314

Listing Expiration 2026-12-31

Marketing Start 2023-08-07

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 71610945

Hyphenated Format 71610-945

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 ANDA209314 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

750 mg/1

source: ndc

Packaging

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-945-30)
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-945-53)
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-945-60)
120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-945-70)

source: ndc

Packages (4)

71610-945-30 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-945-30) 71610-945-53 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-945-53) 71610-945-60 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-945-60) 71610-945-70 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-945-70)

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": "3dfac7d8-fe2d-eb9d-e063-6394a90a477a", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["628953"], "spl_set_id": ["3dfac7ca-2c2e-e709-e063-6394a90adbb3"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-945-30)", "package_ndc": "71610-945-30", "marketing_start_date": "20250903"}, {"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-945-53)", "package_ndc": "71610-945-53", "marketing_start_date": "20250903"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-945-60)", "package_ndc": "71610-945-60", "marketing_start_date": "20250903"}, {"sample": false, "description": "120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-945-70)", "package_ndc": "71610-945-70", "marketing_start_date": "20250903"}], "brand_name": "Potassium Chloride", "product_id": "71610-945_3dfac7d8-fe2d-eb9d-e063-6394a90a477a", "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": "71610-945", "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": "ANDA209314", "marketing_category": "ANDA", "marketing_start_date": "20230807", "listing_expiration_date": "20261231"}