klor-con

Generic: potassium chloride

Labeler: upsher-smith laboratories, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name klor-con
Generic Name potassium chloride
Labeler upsher-smith laboratories, llc
Dosage Form POWDER, FOR SOLUTION
Routes
ORAL
Active Ingredients

potassium chloride 1.5 g/1

Manufacturer
Upsher-Smith Laboratories, LLC

Identifiers & Regulatory

Product NDC 0245-0360
Product ID 0245-0360_39e79418-0497-2b5e-e063-6394a90a4f3a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209662
Listing Expiration 2026-12-31
Marketing Start 2017-10-23

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 02450360
Hyphenated Format 0245-0360

Supplemental Identifiers

RxCUI
1867544 1867547
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 klor-con (source: ndc)
Generic Name potassium chloride (source: ndc)
Application Number ANDA209662 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1.5 g/1
source: ndc
Packaging
  • 100 PACKET in 1 CARTON (0245-0360-01) / 1 POWDER, FOR SOLUTION in 1 PACKET (0245-0360-89)
  • 30 PACKET in 1 CARTON (0245-0360-30) / 1 POWDER, FOR SOLUTION in 1 PACKET (0245-0360-89)
source: ndc

Packages (2)

0245-0360-01 100 PACKET in 1 CARTON (0245-0360-01) / 1 POWDER, FOR SOLUTION in 1 PACKET (0245-0360-89) 0245-0360-30 30 PACKET in 1 CARTON (0245-0360-30) / 1 POWDER, FOR SOLUTION in 1 PACKET (0245-0360-89)

Ingredients (1)

potassium chloride (1.5 g/1)

Linked Drug Pages (1)

KLOR-CON ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "39e79418-0497-2b5e-e063-6394a90a4f3a", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1867544", "1867547"], "spl_set_id": ["e61a4522-b91d-400a-952c-6f035e4610dd"], "manufacturer_name": ["Upsher-Smith Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 PACKET in 1 CARTON (0245-0360-01)  / 1 POWDER, FOR SOLUTION in 1 PACKET (0245-0360-89)", "package_ndc": "0245-0360-01", "marketing_start_date": "20171023"}, {"sample": false, "description": "30 PACKET in 1 CARTON (0245-0360-30)  / 1 POWDER, FOR SOLUTION in 1 PACKET (0245-0360-89)", "package_ndc": "0245-0360-30", "marketing_start_date": "20171023"}], "brand_name": "KLOR-CON", "product_id": "0245-0360_39e79418-0497-2b5e-e063-6394a90a4f3a", "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": "0245-0360", "generic_name": "potassium chloride", "labeler_name": "Upsher-Smith Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "KLOR-CON", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1.5 g/1"}], "application_number": "ANDA209662", "marketing_category": "ANDA", "marketing_start_date": "20171023", "listing_expiration_date": "20261231"}