Package 50268-671-13

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 50268-671-13
Digits Only 5026867113
Product NDC 50268-671
Product ID 50268-671_43f8fa10-9261-a4f3-e063-6394a90a9e93
Description

30 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-671-13) / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (50268-671-11)

Marketing

Marketing Status
Marketed Since 2016-01-28
Brand potassium chloride
Generic potassium chloride
Sample Package No

Linked Drug Pages (1)

Potassium Chloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "43f8fa10-9261-a4f3-e063-6394a90a9e93", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["312504"], "spl_set_id": ["6bb3f62d-79ce-cee6-8c6c-ee1eb6121f01"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-671-13)  / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (50268-671-11)", "package_ndc": "50268-671-13", "marketing_start_date": "20160128"}], "brand_name": "Potassium Chloride", "product_id": "50268-671_43f8fa10-9261-a4f3-e063-6394a90a9e93", "dosage_form": "CAPSULE, 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": "50268-671", "generic_name": "Potassium Chloride", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA202128", "marketing_category": "ANDA", "marketing_start_date": "20160128", "listing_expiration_date": "20261231"}