Package 42291-507-50

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 42291-507-50
Digits Only 4229150750
Product NDC 42291-507
Product ID 42291-507_3a9ebf8f-9705-f72c-e063-6294a90a715a
Description

500 TABLET, EXTENDED RELEASE in 1 BOTTLE (42291-507-50)

Marketing

Marketing Status
Marketed Since 2019-06-19
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": "3a9ebf8f-9705-f72c-e063-6294a90a715a", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1801294"], "spl_set_id": ["8baf3f25-c78b-6c08-e053-2995a90a667e"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (42291-507-01)", "package_ndc": "42291-507-01", "marketing_start_date": "20190619"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (42291-507-50)", "package_ndc": "42291-507-50", "marketing_start_date": "20190619"}], "brand_name": "Potassium Chloride", "product_id": "42291-507_3a9ebf8f-9705-f72c-e063-6294a90a715a", "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": "42291-507", "generic_name": "potassium chloride", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1500 mg/1"}], "application_number": "ANDA074726", "marketing_category": "ANDA", "marketing_start_date": "20190619", "listing_expiration_date": "20261231"}