Package 71610-945-30

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 71610-945-30
Digits Only 7161094530
Product NDC 71610-945
Product ID 71610-945_3dfac7d8-fe2d-eb9d-e063-6394a90a477a
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-945-30)

Marketing

Marketing Status
Marketed Since 2025-09-03
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": "3dfac7d8-fe2d-eb9d-e063-6394a90a477a", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["628953"], "spl_set_id": ["3dfac7ca-2c2e-e709-e063-6394a90adbb3"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-945-30)", "package_ndc": "71610-945-30", "marketing_start_date": "20250903"}, {"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-945-53)", "package_ndc": "71610-945-53", "marketing_start_date": "20250903"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-945-60)", "package_ndc": "71610-945-60", "marketing_start_date": "20250903"}, {"sample": false, "description": "120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-945-70)", "package_ndc": "71610-945-70", "marketing_start_date": "20250903"}], "brand_name": "Potassium Chloride", "product_id": "71610-945_3dfac7d8-fe2d-eb9d-e063-6394a90a477a", "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": "71610-945", "generic_name": "Potassium Chloride", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA209314", "marketing_category": "ANDA", "marketing_start_date": "20230807", "listing_expiration_date": "20261231"}