Package 31722-133-05
Brand: potassium chloride
Generic: potassium chloridePackage Facts
Identity
Package NDC
31722-133-05
Digits Only
3172213305
Product NDC
31722-133
Description
500 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-133-05)
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": "54ef7636-02b5-4062-9171-625d089ebfce", "openfda": {"upc": ["0331722135016", "0331722135054", "0331722134019", "0331722133012", "0331722133050"], "unii": ["660YQ98I10"], "rxcui": ["403888", "1801294", "1801298"], "spl_set_id": ["b1e827aa-b2fb-4fa5-984d-ddd94338ff53"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-133-01)", "package_ndc": "31722-133-01", "marketing_start_date": "20210120"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-133-05)", "package_ndc": "31722-133-05", "marketing_start_date": "20210120"}], "brand_name": "POTASSIUM CHLORIDE", "product_id": "31722-133_54ef7636-02b5-4062-9171-625d089ebfce", "dosage_form": "TABLET, EXTENDED RELEASE", "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": "31722-133", "generic_name": "Potassium CHLORIDE", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CHLORIDE", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA214422", "marketing_category": "ANDA", "marketing_start_date": "20210120", "listing_expiration_date": "20261231"}