Package 51655-706-52

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 51655-706-52
Digits Only 5165570652
Product NDC 51655-706
Product ID 51655-706_4950fc40-5666-f50b-e063-6394a90a7b96
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-706-52)

Marketing

Marketing Status
Marketed Since 2021-04-30
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": "4950fc40-5666-f50b-e063-6394a90a7b96", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["628953"], "spl_set_id": ["db4dc4ab-e0d4-7dc7-e053-2995a90ac46e"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-706-52)", "package_ndc": "51655-706-52", "marketing_start_date": "20210430"}], "brand_name": "Potassium Chloride", "product_id": "51655-706_4950fc40-5666-f50b-e063-6394a90a7b96", "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": "51655-706", "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": "ANDA210733", "marketing_category": "ANDA", "marketing_start_date": "20210430", "listing_expiration_date": "20271231"}