Package 72603-407-03
Brand: potassium chloride
Generic: potassium chloridePackage Facts
Identity
Package NDC
72603-407-03
Digits Only
7260340703
Product NDC
72603-407
Description
100 POUCH in 1 CARTON (72603-407-03) / 1.58 g in 1 POUCH
Marketing
Marketing Status
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": "40906ffd-2143-5419-e063-6294a90a8f27", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1867544"], "spl_set_id": ["fbed8c29-b3f1-4e53-b290-6f717290cecf"], "manufacturer_name": ["Northstar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1.58 g in 1 POUCH (72603-407-01)", "package_ndc": "72603-407-01", "marketing_start_date": "20251006"}, {"sample": false, "description": "30 POUCH in 1 CARTON (72603-407-02) / 1.58 g in 1 POUCH", "package_ndc": "72603-407-02", "marketing_start_date": "20251006"}, {"sample": false, "description": "100 POUCH in 1 CARTON (72603-407-03) / 1.58 g in 1 POUCH", "package_ndc": "72603-407-03", "marketing_start_date": "20251006"}], "brand_name": "Potassium Chloride", "product_id": "72603-407_40906ffd-2143-5419-e063-6294a90a8f27", "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": "72603-407", "generic_name": "Potassium Chloride", "labeler_name": "Northstar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1.5 g/1.58g"}], "application_number": "ANDA214108", "marketing_category": "ANDA", "marketing_start_date": "20251006", "listing_expiration_date": "20261231"}