Package 29300-192-13

Brand: losartan potassium and hydrochlorothiazide

Generic: losartan potassium and hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 29300-192-13
Digits Only 2930019213
Product NDC 29300-192
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-192-13)

Marketing

Marketing Status
Marketed Since 2018-01-15
Brand losartan potassium and hydrochlorothiazide
Generic losartan potassium and hydrochlorothiazide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ad6e4664-08b6-4480-a1fb-6663c8024fef", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0329300190137", "0329300191134", "0329300192131"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979464", "979468", "979471"], "spl_set_id": ["f61b4ffe-cca6-482d-88fa-adf22cb3fff2"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Unichem Pharmaceuticals (USA), Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-192-01)", "package_ndc": "29300-192-01", "marketing_start_date": "20180115"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-192-10)", "package_ndc": "29300-192-10", "marketing_start_date": "20180115"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-192-13)", "package_ndc": "29300-192-13", "marketing_start_date": "20180115"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-192-19)", "package_ndc": "29300-192-19", "marketing_start_date": "20180115"}], "brand_name": "losartan potassium and hydrochlorothiazide", "product_id": "29300-192_ad6e4664-08b6-4480-a1fb-6663c8024fef", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "29300-192", "generic_name": "losartan potassium and hydrochlorothiazide", "labeler_name": "Unichem Pharmaceuticals (USA), Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "losartan potassium and hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}, {"name": "LOSARTAN POTASSIUM", "strength": "100 mg/1"}], "application_number": "ANDA204832", "marketing_category": "ANDA", "marketing_start_date": "20170721", "listing_expiration_date": "20261231"}