potassium chloride

Generic: potassium chloride

Labeler: amneal pharmaceuticals ny llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler amneal pharmaceuticals ny llc
Dosage Form FOR SOLUTION
Routes
ORAL
Active Ingredients

potassium chloride 1.5 g/1.58g

Manufacturer
Amneal Pharmaceuticals NY LLC

Identifiers & Regulatory

Product NDC 60219-1617
Product ID 60219-1617_21ca4401-7e47-41a4-9e08-96f2c300dbbf
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210902
Listing Expiration 2026-12-31
Marketing Start 2023-11-25

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 602191617
Hyphenated Format 60219-1617

Supplemental Identifiers

RxCUI
1867544
UPC
0360219161719 0360219161733
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 ANDA210902 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1.5 g/1.58g
source: ndc
Packaging
  • 30 POUCH in 1 CARTON (60219-1617-3) / 1.58 g in 1 POUCH (60219-1617-1)
  • 100 POUCH in 1 CARTON (60219-1617-8) / 1.58 g in 1 POUCH (60219-1617-1)
source: ndc

Packages (2)

60219-1617-3 30 POUCH in 1 CARTON (60219-1617-3) / 1.58 g in 1 POUCH (60219-1617-1) 60219-1617-8 100 POUCH in 1 CARTON (60219-1617-8) / 1.58 g in 1 POUCH (60219-1617-1)

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": "21ca4401-7e47-41a4-9e08-96f2c300dbbf", "openfda": {"upc": ["0360219161719", "0360219161733"], "unii": ["660YQ98I10"], "rxcui": ["1867544"], "spl_set_id": ["f9965f73-e189-423f-bd10-c4a0ed12b485"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 POUCH in 1 CARTON (60219-1617-3)  / 1.58 g in 1 POUCH (60219-1617-1)", "package_ndc": "60219-1617-3", "marketing_start_date": "20231125"}, {"sample": false, "description": "100 POUCH in 1 CARTON (60219-1617-8)  / 1.58 g in 1 POUCH (60219-1617-1)", "package_ndc": "60219-1617-8", "marketing_start_date": "20231125"}], "brand_name": "Potassium Chloride", "product_id": "60219-1617_21ca4401-7e47-41a4-9e08-96f2c300dbbf", "dosage_form": "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": "60219-1617", "generic_name": "Potassium Chloride", "labeler_name": "Amneal Pharmaceuticals NY LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1.5 g/1.58g"}], "application_number": "ANDA210902", "marketing_category": "ANDA", "marketing_start_date": "20231125", "listing_expiration_date": "20261231"}