potassium chloride for oral solution (10135-807)

Drug Facts

Product Profile

Brand Name potassium chloride for oral solution

Generic Name potassium chloride for oral solution

Labeler marlex pharmaceuticals, inc.

Dosage Form POWDER, FOR SOLUTION

Routes

ORAL

Active Ingredients

potassium chloride 1.5 g/1.58g

Manufacturer

Marlex Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 10135-807

Product ID 10135-807_3e8a7f18-164c-7766-e063-6394a90acbca

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA212183

Listing Expiration 2026-12-31

Marketing Start 2025-08-01

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 10135807

Hyphenated Format 10135-807

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 for oral solution (source: ndc)

Generic Name potassium chloride for oral solution (source: ndc)

Application Number ANDA212183 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

1.5 g/1.58g

source: ndc

Packaging

100 POUCH in 1 CARTON (10135-807-13) / 1.58 g in 1 POUCH (10135-807-11)
30 POUCH in 1 CARTON (10135-807-15) / 1.58 g in 1 POUCH (10135-807-11)

source: ndc

Packages (2)

10135-807-13 100 POUCH in 1 CARTON (10135-807-13) / 1.58 g in 1 POUCH (10135-807-11) 10135-807-15 30 POUCH in 1 CARTON (10135-807-15) / 1.58 g in 1 POUCH (10135-807-11)

Ingredients (1)

potassium chloride (1.5 g/1.58g)

Linked Drug Pages (1)

Potassium Chloride for Oral Solution ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "3e8a7f18-164c-7766-e063-6394a90acbca", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1867544"], "spl_set_id": ["3e8a6f61-44eb-4b5a-e063-6294a90a4b1b"], "manufacturer_name": ["Marlex Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 CARTON (10135-807-13)  / 1.58 g in 1 POUCH (10135-807-11)", "package_ndc": "10135-807-13", "marketing_start_date": "20250801"}, {"sample": false, "description": "30 POUCH in 1 CARTON (10135-807-15)  / 1.58 g in 1 POUCH (10135-807-11)", "package_ndc": "10135-807-15", "marketing_start_date": "20250801"}], "brand_name": "Potassium Chloride for Oral Solution", "product_id": "10135-807_3e8a7f18-164c-7766-e063-6394a90acbca", "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": "10135-807", "generic_name": "Potassium Chloride for Oral Solution", "labeler_name": "Marlex Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride for Oral Solution", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1.5 g/1.58g"}], "application_number": "ANDA212183", "marketing_category": "ANDA", "marketing_start_date": "20250801", "listing_expiration_date": "20261231"}