Package 51655-463-84

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 51655-463-84
Digits Only 5165546384
Product NDC 51655-463
Product ID 51655-463_490f0d08-9a3e-4f23-e063-6294a90a024a
Description

14 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-463-84)

Marketing

Marketing Status
Marketed Since 2020-10-29
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": "490f0d08-9a3e-4f23-e063-6294a90a024a", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["628953"], "spl_set_id": ["f3081031-8234-5732-e053-2995a90aebeb"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-463-84)", "package_ndc": "51655-463-84", "marketing_start_date": "20201029"}], "brand_name": "Potassium Chloride", "product_id": "51655-463_490f0d08-9a3e-4f23-e063-6294a90a024a", "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": "51655-463", "generic_name": "Potassium Chloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA210921", "marketing_category": "ANDA", "marketing_start_date": "20201029", "listing_expiration_date": "20271231"}