Package 43386-915-10

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 43386-915-10
Digits Only 4338691510
Product NDC 43386-915
Product ID 43386-915_a056d531-3e7b-4598-a042-0d498456be72
Description

1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (43386-915-10)

Marketing

Marketing Status
Marketed Since 2017-01-30
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": "a056d531-3e7b-4598-a042-0d498456be72", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1801294", "1801298"], "spl_set_id": ["fe08221d-74d5-490a-8db4-eaf3ed20b289"], "manufacturer_name": ["Lupin Pharmaceuticals,Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (43386-915-01)", "package_ndc": "43386-915-01", "marketing_start_date": "20160121"}, {"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (43386-915-10)", "package_ndc": "43386-915-10", "marketing_start_date": "20170130"}], "brand_name": "Potassium Chloride", "product_id": "43386-915_a056d531-3e7b-4598-a042-0d498456be72", "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": "43386-915", "generic_name": "Potassium Chloride", "labeler_name": "Lupin Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "10 meq/1"}], "application_number": "ANDA206347", "marketing_category": "ANDA", "marketing_start_date": "20160121", "listing_expiration_date": "20261231"}