Package 71205-090-90

Brand: hydrochlorothiazide

Generic: hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 71205-090-90
Digits Only 7120509090
Product NDC 71205-090
Product ID 71205-090_0965a94d-06e5-460f-8edc-d402412da5ee
Description

90 TABLET in 1 BOTTLE (71205-090-90)

Marketing

Marketing Status
Marketed Since 2018-08-01
Brand hydrochlorothiazide
Generic hydrochlorothiazide
Sample Package No

Linked Drug Pages (1)

Hydrochlorothiazide ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0965a94d-06e5-460f-8edc-d402412da5ee", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0371205090906"], "unii": ["0J48LPH2TH"], "rxcui": ["197770"], "spl_set_id": ["48b4d633-ecfa-4748-80e8-6c0e3d8b067e"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71205-090-00)", "package_ndc": "71205-090-00", "marketing_start_date": "20180801"}, {"sample": false, "description": "3 TABLET in 1 BOTTLE (71205-090-03)", "package_ndc": "71205-090-03", "marketing_start_date": "20180801"}, {"sample": false, "description": "7 TABLET in 1 BOTTLE (71205-090-07)", "package_ndc": "71205-090-07", "marketing_start_date": "20180801"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (71205-090-10)", "package_ndc": "71205-090-10", "marketing_start_date": "20180801"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-090-30)", "package_ndc": "71205-090-30", "marketing_start_date": "20180801"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-090-60)", "package_ndc": "71205-090-60", "marketing_start_date": "20180801"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-090-90)", "package_ndc": "71205-090-90", "marketing_start_date": "20180801"}], "brand_name": "Hydrochlorothiazide", "product_id": "71205-090_0965a94d-06e5-460f-8edc-d402412da5ee", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "71205-090", "generic_name": "Hydrochlorothiazide", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "50 mg/1"}], "application_number": "ANDA202556", "marketing_category": "ANDA", "marketing_start_date": "20130410", "listing_expiration_date": "20261231"}