potassium chloride

Generic: potassium chloride

Labeler: kesin pharma corporation
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler kesin pharma corporation
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

potassium chloride 1.5 g/15mL

Manufacturer
Kesin Pharma Corporation

Identifiers & Regulatory

Product NDC 81033-220
Product ID 81033-220_137da9b4-83f0-355f-e063-6294a90af512
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211648
Listing Expiration 2026-12-31
Marketing Start 2022-08-15

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 81033220
Hyphenated Format 81033-220

Supplemental Identifiers

RxCUI
312515
UPC
0381033220512 0381033220529 0381033240510 0381033240503
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 ANDA211648 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1.5 g/15mL
source: ndc
Packaging
  • 10 TRAY in 1 CASE (81033-220-51) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (81033-220-15)
  • 5 TRAY in 1 CASE (81033-220-52) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (81033-220-15)
source: ndc

Packages (2)

81033-220-51 10 TRAY in 1 CASE (81033-220-51) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (81033-220-15) 81033-220-52 5 TRAY in 1 CASE (81033-220-52) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (81033-220-15)

Ingredients (1)

potassium chloride (1.5 g/15mL)

Linked Drug Pages (1)

POTASSIUM CHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "137da9b4-83f0-355f-e063-6294a90af512", "openfda": {"upc": ["0381033220512", "0381033220529", "0381033240510", "0381033240503"], "unii": ["660YQ98I10"], "rxcui": ["312515"], "spl_set_id": ["25c2b417-eeea-4ba6-8eb9-a7d8a08c6093"], "manufacturer_name": ["Kesin Pharma Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 TRAY in 1 CASE (81033-220-51)  / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (81033-220-15)", "package_ndc": "81033-220-51", "marketing_start_date": "20220815"}, {"sample": false, "description": "5 TRAY in 1 CASE (81033-220-52)  / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (81033-220-15)", "package_ndc": "81033-220-52", "marketing_start_date": "20220815"}], "brand_name": "POTASSIUM CHLORIDE", "product_id": "81033-220_137da9b4-83f0-355f-e063-6294a90af512", "dosage_form": "SOLUTION", "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": "81033-220", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "Kesin Pharma Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CHLORIDE", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1.5 g/15mL"}], "application_number": "ANDA211648", "marketing_category": "ANDA", "marketing_start_date": "20220815", "listing_expiration_date": "20261231"}