Package 65862-986-80
Brand: potassium chloride
Generic: potassium chloridePackage Facts
Identity
Package NDC
65862-986-80
Digits Only
6586298680
Product NDC
65862-986
Description
80 BLISTER PACK in 1 CARTON (65862-986-80) / 4 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (65862-986-04)
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": "43cc6b36-fcf7-4e43-b66a-00eecc48d0a7", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["312529", "628953"], "spl_set_id": ["d43beabe-b801-4319-ad36-9a80856b94bd"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-986-01)", "package_ndc": "65862-986-01", "marketing_start_date": "20181219"}, {"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-986-05)", "package_ndc": "65862-986-05", "marketing_start_date": "20181219"}, {"sample": false, "description": "120 BLISTER PACK in 1 CARTON (65862-986-12) / 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (65862-986-06)", "package_ndc": "65862-986-12", "marketing_start_date": "20181219"}, {"sample": false, "description": "80 BLISTER PACK in 1 CARTON (65862-986-80) / 4 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (65862-986-04)", "package_ndc": "65862-986-80", "marketing_start_date": "20181219"}], "brand_name": "Potassium Chloride", "product_id": "65862-986_43cc6b36-fcf7-4e43-b66a-00eecc48d0a7", "dosage_form": "TABLET, FILM COATED, 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": "65862-986", "generic_name": "Potassium Chloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "600 mg/1"}], "application_number": "ANDA210921", "marketing_category": "ANDA", "marketing_start_date": "20181219", "listing_expiration_date": "20261231"}