Package 50090-3700-2

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 50090-3700-2
Digits Only 5009037002
Product NDC 50090-3700
Description

90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50090-3700-2)

Marketing

Marketing Status
Marketed Since 2016-07-26
Brand potassium chloride
Generic potassium chloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3bb0ccdf-d00a-406b-ab2e-6890385d201f", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1801294"], "spl_set_id": ["3a720078-f455-44ab-a883-e3c13d83a74c"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-3700-0)", "package_ndc": "50090-3700-0", "marketing_start_date": "20181019"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50090-3700-1)", "package_ndc": "50090-3700-1", "marketing_start_date": "20160726"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50090-3700-2)", "package_ndc": "50090-3700-2", "marketing_start_date": "20160726"}], "brand_name": "potassium chloride", "product_id": "50090-3700_3bb0ccdf-d00a-406b-ab2e-6890385d201f", "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": "50090-3700", "generic_name": "potassium chloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "potassium chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1500 mg/1"}], "application_number": "ANDA203562", "marketing_category": "ANDA", "marketing_start_date": "20160726", "listing_expiration_date": "20261231"}