klor-con m

Generic: potassium chloride

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

Drug Facts

Product Profile

Brand Name klor-con m
Generic Name potassium chloride
Labeler upsher-smith laboratories, llc
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 1125 mg/1

Manufacturer
Upsher-Smith Laboratories, LLC

Identifiers & Regulatory

Product NDC 0245-5318
Product ID 0245-5318_39e7acd5-8db4-e5cc-e063-6294a90a6baa
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074726
Listing Expiration 2026-12-31
Marketing Start 2011-01-18

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 02455318
Hyphenated Format 0245-5318

Supplemental Identifiers

RxCUI
403888 832731 1801294 1801295 1801298 1801299
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 m (source: ndc)
Generic Name potassium chloride (source: ndc)
Application Number ANDA074726 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1125 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (0245-5318-01) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0245-5318-89)
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0245-5318-11)
source: ndc

Packages (2)

0245-5318-01 100 BLISTER PACK in 1 CARTON (0245-5318-01) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0245-5318-89) 0245-5318-11 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0245-5318-11)

Ingredients (1)

potassium chloride (1125 mg/1)

Linked Drug Pages (1)

KLOR-CON M ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "39e7acd5-8db4-e5cc-e063-6294a90a6baa", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["403888", "832731", "1801294", "1801295", "1801298", "1801299"], "spl_set_id": ["b89910f6-4ff5-4a62-8269-696f7c10e4f6"], "manufacturer_name": ["Upsher-Smith Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0245-5318-01)  / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0245-5318-89)", "package_ndc": "0245-5318-01", "marketing_start_date": "20190621"}, {"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0245-5318-11)", "package_ndc": "0245-5318-11", "marketing_start_date": "20190621"}], "brand_name": "KLOR-CON M", "product_id": "0245-5318_39e7acd5-8db4-e5cc-e063-6294a90a6baa", "dosage_form": "TABLET, EXTENDED RELEASE", "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": "0245-5318", "generic_name": "potassium chloride", "labeler_name": "Upsher-Smith Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "KLOR-CON M", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1125 mg/1"}], "application_number": "ANDA074726", "marketing_category": "ANDA", "marketing_start_date": "20110118", "listing_expiration_date": "20261231"}