potassium chloride extended-release

Generic: potassium chloride extended-release

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride extended-release
Generic Name potassium chloride extended-release
Labeler proficient rx lp
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 1500 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-824
Product ID 71205-824_2d810852-1a61-4411-a036-0d5c41f03989
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214452
Listing Expiration 2026-12-31
Marketing Start 2021-01-30

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 71205824
Hyphenated Format 71205-824

Supplemental Identifiers

RxCUI
1801294
UPC
0371205824105
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 extended-release (source: ndc)
Generic Name potassium chloride extended-release (source: ndc)
Application Number ANDA214452 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1500 mg/1
source: ndc
Packaging
  • 3 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-824-03)
  • 6 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-824-06)
  • 10 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-824-10)
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-824-30)
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-824-60)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-824-90)
source: ndc

Packages (6)

71205-824-03 3 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-824-03) 71205-824-06 6 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-824-06) 71205-824-10 10 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-824-10) 71205-824-30 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-824-30) 71205-824-60 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-824-60) 71205-824-90 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-824-90)

Ingredients (1)

potassium chloride (1500 mg/1)

Linked Drug Pages (1)

Potassium Chloride Extended-release ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2d810852-1a61-4411-a036-0d5c41f03989", "openfda": {"upc": ["0371205824105"], "unii": ["660YQ98I10"], "rxcui": ["1801294"], "spl_set_id": ["f191b15c-7959-4aa6-a2ef-617cde77c918"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "3 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-824-03)", "package_ndc": "71205-824-03", "marketing_start_date": "20230807"}, {"sample": false, "description": "6 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-824-06)", "package_ndc": "71205-824-06", "marketing_start_date": "20230807"}, {"sample": false, "description": "10 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-824-10)", "package_ndc": "71205-824-10", "marketing_start_date": "20230807"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-824-30)", "package_ndc": "71205-824-30", "marketing_start_date": "20230807"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-824-60)", "package_ndc": "71205-824-60", "marketing_start_date": "20230807"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-824-90)", "package_ndc": "71205-824-90", "marketing_start_date": "20230807"}], "brand_name": "Potassium Chloride Extended-release", "product_id": "71205-824_2d810852-1a61-4411-a036-0d5c41f03989", "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": "71205-824", "generic_name": "Potassium Chloride Extended-release", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride Extended-release", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1500 mg/1"}], "application_number": "ANDA214452", "marketing_category": "ANDA", "marketing_start_date": "20210130", "listing_expiration_date": "20261231"}