klor-con/ef

Generic: potassium bicarbonate

Labeler: upsher-smith laboratories, inc.
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name klor-con/ef
Generic Name potassium bicarbonate
Labeler upsher-smith laboratories, inc.
Dosage Form TABLET, EFFERVESCENT
Routes
ORAL
Active Ingredients

potassium bicarbonate 978 mg/1

Manufacturer
Upsher-Smith Laboratories, Inc.

Identifiers & Regulatory

Product NDC 0245-5326
Product ID 0245-5326_39e79ec3-bfd0-e47d-e063-6294a90a25d4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2014-09-01

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 02455326
Hyphenated Format 0245-5326

Supplemental Identifiers

RxCUI
1088772 1537082
UNII
HM5Z15LEBN

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/ef (source: ndc)
Generic Name potassium bicarbonate (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 978 mg/1
source: ndc
Packaging
  • 100 POUCH in 1 CARTON (0245-5326-01) / 1 TABLET, EFFERVESCENT in 1 POUCH (0245-5326-89)
  • 30 POUCH in 1 CARTON (0245-5326-30) / 1 TABLET, EFFERVESCENT in 1 POUCH (0245-5326-89)
source: ndc

Packages (2)

0245-5326-01 100 POUCH in 1 CARTON (0245-5326-01) / 1 TABLET, EFFERVESCENT in 1 POUCH (0245-5326-89) 0245-5326-30 30 POUCH in 1 CARTON (0245-5326-30) / 1 TABLET, EFFERVESCENT in 1 POUCH (0245-5326-89)

Ingredients (1)

potassium bicarbonate (978 mg/1)

Linked Drug Pages (1)

KLOR-Con/EF ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "39e79ec3-bfd0-e47d-e063-6294a90a25d4", "openfda": {"unii": ["HM5Z15LEBN"], "rxcui": ["1088772", "1537082"], "spl_set_id": ["f9d85c4f-aa46-40b2-ad76-89dbf6ec8e4d"], "manufacturer_name": ["Upsher-Smith Laboratories, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 CARTON (0245-5326-01)  / 1 TABLET, EFFERVESCENT in 1 POUCH (0245-5326-89)", "package_ndc": "0245-5326-01", "marketing_start_date": "20190621"}, {"sample": false, "description": "30 POUCH in 1 CARTON (0245-5326-30)  / 1 TABLET, EFFERVESCENT in 1 POUCH (0245-5326-89)", "package_ndc": "0245-5326-30", "marketing_start_date": "20190621"}], "brand_name": "KLOR-Con/EF", "product_id": "0245-5326_39e79ec3-bfd0-e47d-e063-6294a90a25d4", "dosage_form": "TABLET, EFFERVESCENT", "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": "0245-5326", "generic_name": "Potassium Bicarbonate", "labeler_name": "Upsher-Smith Laboratories, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "KLOR-Con/EF", "active_ingredients": [{"name": "POTASSIUM BICARBONATE", "strength": "978 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20140901", "listing_expiration_date": "20261231"}