Package 71205-015-90

Brand: valsartan and hydrochlorothiazide

Generic: valsartan and hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 71205-015-90
Digits Only 7120501590
Product NDC 71205-015
Description

90 TABLET, FILM COATED in 1 BOTTLE (71205-015-90)

Marketing

Marketing Status
Marketed Since 2018-04-02
Brand valsartan and hydrochlorothiazide
Generic valsartan and hydrochlorothiazide
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fb1db133-2efe-4418-841b-f86104c50170", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776", "N0000000070", "N0000175561"], "unii": ["0J48LPH2TH", "80M03YXJ7I"], "rxcui": ["636045"], "spl_set_id": ["6c363351-6596-42bf-83c9-041bf231b778"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]", "Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-015-30)", "package_ndc": "71205-015-30", "marketing_start_date": "20180402"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-015-60)", "package_ndc": "71205-015-60", "marketing_start_date": "20180402"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-015-90)", "package_ndc": "71205-015-90", "marketing_start_date": "20180402"}], "brand_name": "Valsartan and Hydrochlorothiazide", "product_id": "71205-015_fb1db133-2efe-4418-841b-f86104c50170", "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": "71205-015", "generic_name": "Valsartan and Hydrochlorothiazide", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valsartan and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}, {"name": "VALSARTAN", "strength": "320 mg/1"}], "application_number": "ANDA201662", "marketing_category": "ANDA", "marketing_start_date": "20160520", "listing_expiration_date": "20261231"}