potassium chloride

Generic: potassium chloride

Labeler: endo usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler endo usa, inc.
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

potassium chloride 40 meq/15mL

Manufacturer
Endo USA, Inc.

Identifiers & Regulatory

Product NDC 0603-1543
Product ID 0603-1543_f57f6d4a-b7d8-407b-8259-19dff55a841d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA206814
Marketing Start 2015-05-04
Marketing End 2026-07-31

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 06031543
Hyphenated Format 0603-1543

Supplemental Identifiers

RxCUI
312515 314182
UPC
0306031543586 0306031542589
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 NDA206814 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 meq/15mL
source: ndc
Packaging
  • 473 mL in 1 BOTTLE, PLASTIC (0603-1543-58)
source: ndc

Packages (1)

0603-1543-58 473 mL in 1 BOTTLE, PLASTIC (0603-1543-58)

Ingredients (1)

potassium chloride (40 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": "f57f6d4a-b7d8-407b-8259-19dff55a841d", "openfda": {"upc": ["0306031543586", "0306031542589"], "unii": ["660YQ98I10"], "rxcui": ["312515", "314182"], "spl_set_id": ["e5214432-3517-4a90-9412-036752bd1139"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE, PLASTIC (0603-1543-58)", "package_ndc": "0603-1543-58", "marketing_end_date": "20260731", "marketing_start_date": "20150504"}], "brand_name": "Potassium Chloride", "product_id": "0603-1543_f57f6d4a-b7d8-407b-8259-19dff55a841d", "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": "0603-1543", "generic_name": "Potassium Chloride", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "40 meq/15mL"}], "application_number": "NDA206814", "marketing_category": "NDA", "marketing_end_date": "20260731", "marketing_start_date": "20150504"}