potassium chloride

Generic: potassium chloride

Labeler: genus lifesciences inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler genus lifesciences inc.
Dosage Form POWDER, FOR SOLUTION
Routes
ORAL
Active Ingredients

potassium chloride 1.5 g/1.58g

Manufacturer
Genus Lifesciences Inc.

Identifiers & Regulatory

Product NDC 64950-321
Product ID 64950-321_015c512b-8162-47af-9181-69065eef98fa
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA208019
Listing Expiration 2026-12-31
Marketing Start 2015-09-07

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 64950321
Hyphenated Format 64950-321

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 NDA208019 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1.5 g/1.58g
source: ndc
Packaging
  • 100 POUCH in 1 CARTON (64950-321-01) / 1.58 g in 1 POUCH (64950-321-20)
  • 30 POUCH in 1 CARTON (64950-321-30) / 1.58 g in 1 POUCH (64950-321-20)
source: ndc

Packages (2)

64950-321-01 100 POUCH in 1 CARTON (64950-321-01) / 1.58 g in 1 POUCH (64950-321-20) 64950-321-30 30 POUCH in 1 CARTON (64950-321-30) / 1.58 g in 1 POUCH (64950-321-20)

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": "015c512b-8162-47af-9181-69065eef98fa", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1867544"], "spl_set_id": ["23d818e7-c076-40de-8dc1-0b51ba4be96a"], "manufacturer_name": ["Genus Lifesciences Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 CARTON (64950-321-01)  / 1.58 g in 1 POUCH (64950-321-20)", "package_ndc": "64950-321-01", "marketing_start_date": "20150907"}, {"sample": false, "description": "30 POUCH in 1 CARTON (64950-321-30)  / 1.58 g in 1 POUCH (64950-321-20)", "package_ndc": "64950-321-30", "marketing_start_date": "20150907"}], "brand_name": "Potassium Chloride", "product_id": "64950-321_015c512b-8162-47af-9181-69065eef98fa", "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": "64950-321", "generic_name": "Potassium Chloride", "labeler_name": "Genus Lifesciences Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1.5 g/1.58g"}], "application_number": "NDA208019", "marketing_category": "NDA", "marketing_start_date": "20150907", "listing_expiration_date": "20261231"}