Package 71205-258-90

Brand: valsartan and hydrochlorothiazide

Generic: valsartan and hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 71205-258-90
Digits Only 7120525890
Product NDC 71205-258
Description

90 TABLET, FILM COATED in 1 BOTTLE (71205-258-90)

Marketing

Marketing Status
Marketed Since 2019-05-01
Brand valsartan and hydrochlorothiazide
Generic valsartan and hydrochlorothiazide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "09764c50-8d91-4c74-8d5f-d48f79ecb01c", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776", "N0000000070", "N0000175561"], "upc": ["0371205258306"], "unii": ["0J48LPH2TH", "80M03YXJ7I"], "rxcui": ["200285"], "spl_set_id": ["a9098fc6-3d2a-404f-a4cd-2e181ebbd626"], "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 (71205-258-30)", "package_ndc": "71205-258-30", "marketing_start_date": "20190501"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-258-60)", "package_ndc": "71205-258-60", "marketing_start_date": "20190501"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-258-90)", "package_ndc": "71205-258-90", "marketing_start_date": "20190501"}], "brand_name": "Valsartan and Hydrochlorothiazide", "product_id": "71205-258_09764c50-8d91-4c74-8d5f-d48f79ecb01c", "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": "71205-258", "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": "12.5 mg/1"}, {"name": "VALSARTAN", "strength": "160 mg/1"}], "application_number": "ANDA203145", "marketing_category": "ANDA", "marketing_start_date": "20130419", "listing_expiration_date": "20261231"}