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, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 1500 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1747
Product ID 71335-1747_665b242e-6601-4a0a-af84-338e349e2926
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074726
Listing Expiration 2026-12-31
Marketing Start 1998-11-20

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 713351747
Hyphenated Format 71335-1747

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 ANDA074726 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1500 mg/1
source: ndc
Packaging
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1747-1)
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1747-2)
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1747-3)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1747-4)
  • 15 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1747-5)
  • 7 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1747-6)
  • 10 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1747-7)
  • 3 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1747-8)
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": "665b242e-6601-4a0a-af84-338e349e2926", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1801294"], "spl_set_id": ["0e875691-7372-46ac-80a1-946e08b40061"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1747-1)", "package_ndc": "71335-1747-1", "marketing_start_date": "20201217"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1747-2)", "package_ndc": "71335-1747-2", "marketing_start_date": "20201217"}, {"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1747-3)", "package_ndc": "71335-1747-3", "marketing_start_date": "20201217"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1747-4)", "package_ndc": "71335-1747-4", "marketing_start_date": "20201217"}, {"sample": false, "description": "15 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1747-5)", "package_ndc": "71335-1747-5", "marketing_start_date": "20201217"}, {"sample": false, "description": "7 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1747-6)", "package_ndc": "71335-1747-6", "marketing_start_date": "20201217"}, {"sample": false, "description": "10 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1747-7)", "package_ndc": "71335-1747-7", "marketing_start_date": "20201217"}, {"sample": false, "description": "3 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1747-8)", "package_ndc": "71335-1747-8", "marketing_start_date": "20201217"}], "brand_name": "Potassium Chloride", "product_id": "71335-1747_665b242e-6601-4a0a-af84-338e349e2926", "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": "71335-1747", "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": "1500 mg/1"}], "application_number": "ANDA074726", "marketing_category": "ANDA", "marketing_start_date": "19981120", "listing_expiration_date": "20261231"}