potassium chloride

Generic: potassium chloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler bryant ranch prepack
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 600 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 63629-2620
Product ID 63629-2620_969312e9-8b4a-4f3a-823d-903600206b47
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 636292620
Hyphenated Format 63629-2620

Supplemental Identifiers

RxCUI
312529
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
  • 600 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-1)
  • 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-2)
  • 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-3)
  • 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-4)
  • 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-5)
source: ndc

Packages (5)

63629-2620-1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-1) 63629-2620-2 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-2) 63629-2620-3 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-3) 63629-2620-4 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-4) 63629-2620-5 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-5)

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": "969312e9-8b4a-4f3a-823d-903600206b47", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["312529"], "spl_set_id": ["9088ca44-5585-4551-8e2c-168f306520d4"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-1)", "package_ndc": "63629-2620-1", "marketing_start_date": "20240206"}, {"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-2)", "package_ndc": "63629-2620-2", "marketing_start_date": "20240206"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-3)", "package_ndc": "63629-2620-3", "marketing_start_date": "20240206"}, {"sample": false, "description": "180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-4)", "package_ndc": "63629-2620-4", "marketing_start_date": "20240206"}, {"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-5)", "package_ndc": "63629-2620-5", "marketing_start_date": "20240206"}], "brand_name": "Potassium Chloride", "product_id": "63629-2620_969312e9-8b4a-4f3a-823d-903600206b47", "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": "63629-2620", "generic_name": "Potassium Chloride", "labeler_name": "Bryant Ranch Prepack", "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"}