potassium chloride

Generic: potassium chloride

Labeler: northstar rx llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

potassium chloride 1.5 g/1.58g

Manufacturer
Northstar Rx LLC

Identifiers & Regulatory

Product NDC 72603-407
Product ID 72603-407_40906ffd-2143-5419-e063-6294a90a8f27
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214108
Listing Expiration 2026-12-31
Marketing Start 2025-10-06

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 72603407
Hyphenated Format 72603-407

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 ANDA214108 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1.5 g/1.58g
source: ndc
Packaging
  • 1.58 g in 1 POUCH (72603-407-01)
  • 30 POUCH in 1 CARTON (72603-407-02) / 1.58 g in 1 POUCH
  • 100 POUCH in 1 CARTON (72603-407-03) / 1.58 g in 1 POUCH
source: ndc

Packages (3)

72603-407-01 1.58 g in 1 POUCH (72603-407-01) 72603-407-02 30 POUCH in 1 CARTON (72603-407-02) / 1.58 g in 1 POUCH 72603-407-03 100 POUCH in 1 CARTON (72603-407-03) / 1.58 g in 1 POUCH

Ingredients (1)

potassium chloride (1.5 g/1.58g)

Linked Drug Pages (1)

Potassium Chloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "40906ffd-2143-5419-e063-6294a90a8f27", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1867544"], "spl_set_id": ["fbed8c29-b3f1-4e53-b290-6f717290cecf"], "manufacturer_name": ["Northstar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1.58 g in 1 POUCH (72603-407-01)", "package_ndc": "72603-407-01", "marketing_start_date": "20251006"}, {"sample": false, "description": "30 POUCH in 1 CARTON (72603-407-02)  / 1.58 g in 1 POUCH", "package_ndc": "72603-407-02", "marketing_start_date": "20251006"}, {"sample": false, "description": "100 POUCH in 1 CARTON (72603-407-03)  / 1.58 g in 1 POUCH", "package_ndc": "72603-407-03", "marketing_start_date": "20251006"}], "brand_name": "Potassium Chloride", "product_id": "72603-407_40906ffd-2143-5419-e063-6294a90a8f27", "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": "72603-407", "generic_name": "Potassium Chloride", "labeler_name": "Northstar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1.5 g/1.58g"}], "application_number": "ANDA214108", "marketing_category": "ANDA", "marketing_start_date": "20251006", "listing_expiration_date": "20261231"}