potassium chloride

Generic: potassium chloride

Labeler: kesin pharma corporation
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler kesin pharma corporation
Dosage Form POWDER, FOR SOLUTION
Routes
ORAL
Active Ingredients

potassium chloride 1.5 g/1.58g

Manufacturer
Kesin Pharma Corporation

Identifiers & Regulatory

Product NDC 81033-413
Product ID 81033-413_440dbe01-dea3-0833-e063-6394a90ab048
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211667
Listing Expiration 2026-12-31
Marketing Start 2022-10-24

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 81033413
Hyphenated Format 81033-413

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 ANDA211667 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1.5 g/1.58g
source: ndc
Packaging
  • 100 POUCH in 1 CARTON (81033-413-01) / 1.58 g in 1 POUCH (81033-413-20)
source: ndc

Packages (1)

81033-413-01 100 POUCH in 1 CARTON (81033-413-01) / 1.58 g in 1 POUCH (81033-413-20)

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": "440dbe01-dea3-0833-e063-6394a90ab048", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1867544"], "spl_set_id": ["440dcbbb-bb31-d3fd-e063-6294a90ab2f7"], "manufacturer_name": ["Kesin Pharma Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 CARTON (81033-413-01)  / 1.58 g in 1 POUCH (81033-413-20)", "package_ndc": "81033-413-01", "marketing_start_date": "20250901"}], "brand_name": "Potassium Chloride", "product_id": "81033-413_440dbe01-dea3-0833-e063-6394a90ab048", "dosage_form": "POWDER, FOR SOLUTION", "product_ndc": "81033-413", "generic_name": "Potassium Chloride", "labeler_name": "Kesin Pharma Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1.5 g/1.58g"}], "application_number": "ANDA211667", "marketing_category": "ANDA", "marketing_start_date": "20221024", "listing_expiration_date": "20261231"}