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 TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 750 mg/1

Manufacturer
Northstar Rx LLC

Identifiers & Regulatory

Product NDC 72603-337
Product ID 72603-337_2087e0c5-7d3f-48dd-823d-5b4f72beb998
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214422
Listing Expiration 2026-12-31
Marketing Start 2024-06-21

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 72603337
Hyphenated Format 72603-337

Supplemental Identifiers

RxCUI
1801294 1801298
UPC
0372603337013
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 ANDA214422 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72603-337-01)
source: ndc

Packages (1)

72603-337-01 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72603-337-01)

Ingredients (1)

potassium chloride (750 mg/1)

Linked Drug Pages (1)

potassium chloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2087e0c5-7d3f-48dd-823d-5b4f72beb998", "openfda": {"upc": ["0372603337013"], "unii": ["660YQ98I10"], "rxcui": ["1801294", "1801298"], "spl_set_id": ["b19a3fbf-cdbb-4f86-ac61-5dfb07e0a51a"], "manufacturer_name": ["Northstar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72603-337-01)", "package_ndc": "72603-337-01", "marketing_start_date": "20240621"}], "brand_name": "potassium chloride", "product_id": "72603-337_2087e0c5-7d3f-48dd-823d-5b4f72beb998", "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": "72603-337", "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": "750 mg/1"}], "application_number": "ANDA214422", "marketing_category": "ANDA", "marketing_start_date": "20240621", "listing_expiration_date": "20261231"}