Package 62332-080-90

Brand: valsartan and hydrochlorothiazide

Generic: valsartan and hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 62332-080-90
Digits Only 6233208090
Product NDC 62332-080
Description

90 TABLET, FILM COATED in 1 BOTTLE (62332-080-90)

Marketing

Marketing Status
Marketed Since 2016-05-20
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": "29d9e9d2-2c11-49c0-b397-cd429cf701df", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776", "N0000000070", "N0000175561"], "upc": ["0362332082902", "0362332079308", "0362332081301"], "unii": ["0J48LPH2TH", "80M03YXJ7I"], "rxcui": ["200284", "200285", "349353", "636042", "636045"], "spl_set_id": ["973973a3-9fec-4afc-910f-187f099dfe2d"], "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": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 CARTON (62332-080-10)", "package_ndc": "62332-080-10", "marketing_start_date": "20160520"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (62332-080-30)", "package_ndc": "62332-080-30", "marketing_start_date": "20160520"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (62332-080-71)", "package_ndc": "62332-080-71", "marketing_start_date": "20160520"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (62332-080-90)", "package_ndc": "62332-080-90", "marketing_start_date": "20160520"}], "brand_name": "Valsartan and Hydrochlorothiazide", "product_id": "62332-080_29d9e9d2-2c11-49c0-b397-cd429cf701df", "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": "62332-080", "generic_name": "Valsartan and Hydrochlorothiazide", "labeler_name": "Alembic Pharmaceuticals Inc.", "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": "ANDA201662", "marketing_category": "ANDA", "marketing_start_date": "20160520", "listing_expiration_date": "20261231"}