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 71610-632
Product ID 71610-632_43fa1a49-9d48-17b2-e063-6394a90ac4f4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214422
Listing Expiration 2026-12-31
Marketing Start 2021-01-20

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 71610632
Hyphenated Format 71610-632

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 ANDA214422 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1500 mg/1
source: ndc
Packaging
  • 15 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-632-15)
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-632-30)
  • 45 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-632-45)
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-632-53)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-632-60)
  • 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-632-70)
  • 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-632-80)
  • 270 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-632-92)
source: ndc

Packages (8)

Ingredients (1)

potassium chloride (1500 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "43fa1a49-9d48-17b2-e063-6394a90ac4f4", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1801294"], "spl_set_id": ["61fe55c2-fc9a-4fae-899a-06601baa78e1"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-632-15)", "package_ndc": "71610-632-15", "marketing_start_date": "20220204"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-632-30)", "package_ndc": "71610-632-30", "marketing_start_date": "20220204"}, {"sample": false, "description": "45 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-632-45)", "package_ndc": "71610-632-45", "marketing_start_date": "20220204"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-632-53)", "package_ndc": "71610-632-53", "marketing_start_date": "20220204"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-632-60)", "package_ndc": "71610-632-60", "marketing_start_date": "20220204"}, {"sample": false, "description": "120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-632-70)", "package_ndc": "71610-632-70", "marketing_start_date": "20251119"}, {"sample": false, "description": "180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-632-80)", "package_ndc": "71610-632-80", "marketing_start_date": "20220204"}, {"sample": false, "description": "270 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-632-92)", "package_ndc": "71610-632-92", "marketing_start_date": "20250421"}], "brand_name": "POTASSIUM CHLORIDE", "product_id": "71610-632_43fa1a49-9d48-17b2-e063-6394a90ac4f4", "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": "71610-632", "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": "ANDA214422", "marketing_category": "ANDA", "marketing_start_date": "20210120", "listing_expiration_date": "20261231"}