potassium chloride

Generic: potassium chloride

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler aurobindo pharma limited
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 600 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 65862-986
Product ID 65862-986_43cc6b36-fcf7-4e43-b66a-00eecc48d0a7
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 65862986
Hyphenated Format 65862-986

Supplemental Identifiers

RxCUI
312529 628953
UNII
660YQ98I10

Packaging Origin

Original Packager
true

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
  • 600 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-986-01)
  • 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-986-05)
  • 120 BLISTER PACK in 1 CARTON (65862-986-12) / 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (65862-986-06)
  • 80 BLISTER PACK in 1 CARTON (65862-986-80) / 4 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (65862-986-04)
source: ndc

Packages (4)

65862-986-01 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-986-01) 65862-986-05 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-986-05) 65862-986-12 120 BLISTER PACK in 1 CARTON (65862-986-12) / 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (65862-986-06) 65862-986-80 80 BLISTER PACK in 1 CARTON (65862-986-80) / 4 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (65862-986-04)

Ingredients (1)

potassium chloride (600 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": "43cc6b36-fcf7-4e43-b66a-00eecc48d0a7", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["312529", "628953"], "spl_set_id": ["d43beabe-b801-4319-ad36-9a80856b94bd"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-986-01)", "package_ndc": "65862-986-01", "marketing_start_date": "20181219"}, {"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-986-05)", "package_ndc": "65862-986-05", "marketing_start_date": "20181219"}, {"sample": false, "description": "120 BLISTER PACK in 1 CARTON (65862-986-12)  / 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (65862-986-06)", "package_ndc": "65862-986-12", "marketing_start_date": "20181219"}, {"sample": false, "description": "80 BLISTER PACK in 1 CARTON (65862-986-80)  / 4 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (65862-986-04)", "package_ndc": "65862-986-80", "marketing_start_date": "20181219"}], "brand_name": "Potassium Chloride", "product_id": "65862-986_43cc6b36-fcf7-4e43-b66a-00eecc48d0a7", "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": "65862-986", "generic_name": "Potassium Chloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "600 mg/1"}], "application_number": "ANDA210921", "marketing_category": "ANDA", "marketing_start_date": "20181219", "listing_expiration_date": "20261231"}