Package 43386-169-01

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 43386-169-01
Digits Only 4338616901
Product NDC 43386-169
Product ID 43386-169_b48fb85d-87f5-0c70-e053-2a95a90a7011
Description

473 mL in 1 BOTTLE (43386-169-01)

Marketing

Marketing Status
Marketed Since 2018-09-24
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": "b48fb85d-87f5-0c70-e053-2a95a90a7011", "openfda": {"upc": ["0343386169016", "0343386168019"], "unii": ["660YQ98I10"], "rxcui": ["312515", "314182"], "spl_set_id": ["28c49165-d8c9-443a-b000-953b8e1ec55c"], "manufacturer_name": ["Lupin Pharmaceuticals,Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (43386-169-01)", "package_ndc": "43386-169-01", "marketing_start_date": "20180924"}], "brand_name": "POTASSIUM CHLORIDE", "product_id": "43386-169_b48fb85d-87f5-0c70-e053-2a95a90a7011", "dosage_form": "SOLUTION", "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": "43386-169", "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": "40 meq/15mL"}], "application_number": "ANDA209786", "marketing_category": "ANDA", "marketing_start_date": "20180924", "listing_expiration_date": "20261231"}