Package 65162-847-50
Brand: valsartan and hydrochlorothiazide
Generic: valsartan and hydrochlorothiazidePackage Facts
Identity
Package NDC
65162-847-50
Digits Only
6516284750
Product NDC
65162-847
Description
500 TABLET, FILM COATED in 1 BOTTLE (65162-847-50)
Marketing
Marketing Status
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": "e40f4475-c8d3-48a6-913f-cf7c8c7b119b", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776", "N0000000070", "N0000175561"], "upc": ["0365162849097", "0365162847093", "0365162846096", "0365162848090"], "unii": ["0J48LPH2TH", "80M03YXJ7I"], "rxcui": ["200284", "200285", "349353", "636042", "636045"], "spl_set_id": ["c9acbc95-3629-4276-842b-5c074844dba7"], "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": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (65162-847-03)", "package_ndc": "65162-847-03", "marketing_start_date": "20230814"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (65162-847-09)", "package_ndc": "65162-847-09", "marketing_start_date": "20230814"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (65162-847-11)", "package_ndc": "65162-847-11", "marketing_start_date": "20230814"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (65162-847-50)", "package_ndc": "65162-847-50", "marketing_start_date": "20230814"}], "brand_name": "Valsartan and Hydrochlorothiazide", "product_id": "65162-847_e40f4475-c8d3-48a6-913f-cf7c8c7b119b", "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": "65162-847", "generic_name": "Valsartan and Hydrochlorothiazide", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valsartan and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}, {"name": "VALSARTAN", "strength": "160 mg/1"}], "application_number": "ANDA204382", "marketing_category": "ANDA", "marketing_start_date": "20230814", "listing_expiration_date": "20261231"}