Package 81033-413-01

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 81033-413-01
Digits Only 8103341301
Product NDC 81033-413
Description

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

Marketing

Marketing Status
Marketed Since 2025-09-01
Brand potassium chloride
Generic potassium chloride
Sample Package No

Linked Drug Pages (1)

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"}