potassium chloride extended-release

Generic: potassium chloride

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride extended-release
Generic Name potassium chloride
Labeler a-s medication solutions
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 750 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-6639
Product ID 50090-6639_1f46dbb9-0034-4574-bcd4-1bc9a90529f3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209688
Listing Expiration 2026-12-31
Marketing Start 2023-04-10

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 500906639
Hyphenated Format 50090-6639

Supplemental Identifiers

RxCUI
628953
UNII
660YQ98I10

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 extended-release (source: ndc)
Generic Name potassium chloride (source: ndc)
Application Number ANDA209688 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6639-0)
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6639-1)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6639-2)
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6639-3)
source: ndc

Packages (4)

50090-6639-0 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6639-0) 50090-6639-1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6639-1) 50090-6639-2 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6639-2) 50090-6639-3 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6639-3)

Ingredients (1)

potassium chloride (750 mg/1)

Linked Drug Pages (1)

Potassium Chloride Extended-Release ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1f46dbb9-0034-4574-bcd4-1bc9a90529f3", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["628953"], "spl_set_id": ["d486f982-a7d3-463d-a68d-89365ddaf5bb"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6639-0)", "package_ndc": "50090-6639-0", "marketing_start_date": "20230829"}, {"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6639-1)", "package_ndc": "50090-6639-1", "marketing_start_date": "20230829"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6639-2)", "package_ndc": "50090-6639-2", "marketing_start_date": "20230829"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6639-3)", "package_ndc": "50090-6639-3", "marketing_start_date": "20240112"}], "brand_name": "Potassium Chloride Extended-Release", "product_id": "50090-6639_1f46dbb9-0034-4574-bcd4-1bc9a90529f3", "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": "50090-6639", "generic_name": "Potassium Chloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "brand_name_suffix": "Extended-Release", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA209688", "marketing_category": "ANDA", "marketing_start_date": "20230410", "listing_expiration_date": "20261231"}