potassium chloride

Generic: potassium chloride

Labeler: epic pharma, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler epic pharma, llc
Dosage Form POWDER, FOR SOLUTION
Routes
ORAL
Active Ingredients

potassium chloride 1.5 g/1.77g

Manufacturer
Epic Pharma, LLC

Identifiers & Regulatory

Product NDC 42806-094
Product ID 42806-094_58c7eab4-f697-478c-be72-4cba3e74dc2c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210200
Listing Expiration 2026-12-31
Marketing Start 2018-11-28

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 42806094
Hyphenated Format 42806-094

Supplemental Identifiers

RxCUI
1867544
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 ANDA210200 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1.5 g/1.77g
source: ndc
Packaging
  • 100 PACKET in 1 CARTON (42806-094-01) / 1.77 g in 1 PACKET (42806-094-99)
  • 30 PACKET in 1 CARTON (42806-094-30) / 1.77 g in 1 PACKET (42806-094-99)
source: ndc

Packages (2)

42806-094-01 100 PACKET in 1 CARTON (42806-094-01) / 1.77 g in 1 PACKET (42806-094-99) 42806-094-30 30 PACKET in 1 CARTON (42806-094-30) / 1.77 g in 1 PACKET (42806-094-99)

Ingredients (1)

potassium chloride (1.5 g/1.77g)

Linked Drug Pages (1)

POTASSIUM CHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "58c7eab4-f697-478c-be72-4cba3e74dc2c", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1867544"], "spl_set_id": ["1373321f-533a-4ab4-8bcd-8bde15371a09"], "manufacturer_name": ["Epic Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 PACKET in 1 CARTON (42806-094-01)  / 1.77 g in 1 PACKET (42806-094-99)", "package_ndc": "42806-094-01", "marketing_start_date": "20181128"}, {"sample": false, "description": "30 PACKET in 1 CARTON (42806-094-30)  / 1.77 g in 1 PACKET (42806-094-99)", "package_ndc": "42806-094-30", "marketing_start_date": "20181128"}], "brand_name": "POTASSIUM CHLORIDE", "product_id": "42806-094_58c7eab4-f697-478c-be72-4cba3e74dc2c", "dosage_form": "POWDER, FOR 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": "42806-094", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "Epic Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CHLORIDE", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1.5 g/1.77g"}], "application_number": "ANDA210200", "marketing_category": "ANDA", "marketing_start_date": "20181128", "listing_expiration_date": "20261231"}