Package 71335-2866-1
Brand: potassium chloride extended-release
Generic: potassium chloridePackage Facts
Identity
Package NDC
71335-2866-1
Digits Only
7133528661
Product NDC
71335-2866
Description
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2866-1)
Marketing
Marketing Status
Brand
potassium chloride extended-release
Generic
potassium chloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "af8e2fea-aa03-4fc5-8e9a-2c10ef9ba59e", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1801298"], "spl_set_id": ["6fc9eef0-3dfc-4344-85c7-9f11d9b99b65"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2866-1)", "package_ndc": "71335-2866-1", "marketing_start_date": "20251106"}], "brand_name": "Potassium Chloride Extended-Release", "product_id": "71335-2866_af8e2fea-aa03-4fc5-8e9a-2c10ef9ba59e", "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": "71335-2866", "generic_name": "Potassium Chloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride Extended-Release", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA076368", "marketing_category": "ANDA", "marketing_start_date": "20191120", "listing_expiration_date": "20261231"}