potassium chloride

Generic: potassium chloride

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

Drug Facts

Product Profile

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

potassium chloride 1500 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-3700
Product ID 50090-3700_3bb0ccdf-d00a-406b-ab2e-6890385d201f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203562
Listing Expiration 2026-12-31
Marketing Start 2016-07-26

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 500903700
Hyphenated Format 50090-3700

Supplemental Identifiers

RxCUI
1801294
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 (source: ndc)
Generic Name potassium chloride (source: ndc)
Application Number ANDA203562 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1500 mg/1
source: ndc
Packaging
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-3700-0)
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50090-3700-1)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50090-3700-2)
source: ndc

Packages (3)

50090-3700-0 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-3700-0) 50090-3700-1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50090-3700-1) 50090-3700-2 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50090-3700-2)

Ingredients (1)

potassium chloride (1500 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": "3bb0ccdf-d00a-406b-ab2e-6890385d201f", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1801294"], "spl_set_id": ["3a720078-f455-44ab-a883-e3c13d83a74c"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-3700-0)", "package_ndc": "50090-3700-0", "marketing_start_date": "20181019"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50090-3700-1)", "package_ndc": "50090-3700-1", "marketing_start_date": "20160726"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50090-3700-2)", "package_ndc": "50090-3700-2", "marketing_start_date": "20160726"}], "brand_name": "potassium chloride", "product_id": "50090-3700_3bb0ccdf-d00a-406b-ab2e-6890385d201f", "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": "50090-3700", "generic_name": "potassium chloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "potassium chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1500 mg/1"}], "application_number": "ANDA203562", "marketing_category": "ANDA", "marketing_start_date": "20160726", "listing_expiration_date": "20261231"}