potassium chloride

Generic: potassium chloride

Labeler: guardian drug company
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler guardian drug company
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

potassium chloride 20 meq/15mL

Manufacturer
Guardian Drug Company

Identifiers & Regulatory

Product NDC 53041-681
Product ID 53041-681_859606e1-12d2-4eff-b6f3-4fa59c4da89b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214892
Listing Expiration 2026-12-31
Marketing Start 2021-07-09

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 53041681
Hyphenated Format 53041-681

Supplemental Identifiers

RxCUI
312515 314182
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 ANDA214892 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 meq/15mL
source: ndc
Packaging
  • 473 mL in 1 BOTTLE (53041-681-06)
  • 10 CUP, UNIT-DOSE in 1 TRAY (53041-681-17) / 15 mL in 1 CUP, UNIT-DOSE (53041-681-96)
  • 10 CUP, UNIT-DOSE in 1 TRAY (53041-681-29) / 30 mL in 1 CUP, UNIT-DOSE (53041-681-97)
source: ndc

Packages (3)

53041-681-06 473 mL in 1 BOTTLE (53041-681-06) 53041-681-17 10 CUP, UNIT-DOSE in 1 TRAY (53041-681-17) / 15 mL in 1 CUP, UNIT-DOSE (53041-681-96) 53041-681-29 10 CUP, UNIT-DOSE in 1 TRAY (53041-681-29) / 30 mL in 1 CUP, UNIT-DOSE (53041-681-97)

Ingredients (1)

potassium chloride (20 meq/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": "859606e1-12d2-4eff-b6f3-4fa59c4da89b", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["312515", "314182"], "spl_set_id": ["3d460e84-27a0-485c-8b11-58d03d9064aa"], "manufacturer_name": ["Guardian Drug Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (53041-681-06)", "package_ndc": "53041-681-06", "marketing_start_date": "20210709"}, {"sample": false, "description": "10 CUP, UNIT-DOSE in 1 TRAY (53041-681-17)  / 15 mL in 1 CUP, UNIT-DOSE (53041-681-96)", "package_ndc": "53041-681-17", "marketing_start_date": "20210709"}, {"sample": false, "description": "10 CUP, UNIT-DOSE in 1 TRAY (53041-681-29)  / 30 mL in 1 CUP, UNIT-DOSE (53041-681-97)", "package_ndc": "53041-681-29", "marketing_start_date": "20210709"}], "brand_name": "Potassium Chloride", "product_id": "53041-681_859606e1-12d2-4eff-b6f3-4fa59c4da89b", "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": "53041-681", "generic_name": "Potassium Chloride", "labeler_name": "Guardian Drug Company", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "20 meq/15mL"}], "application_number": "ANDA214892", "marketing_category": "ANDA", "marketing_start_date": "20210709", "listing_expiration_date": "20261231"}