Package 16729-184-17
Brand: hydrochlorothiazide
Generic: hydrochlorothiazidePackage Facts
Identity
Package NDC
16729-184-17
Digits Only
1672918417
Product NDC
16729-184
Description
1000 TABLET in 1 BOTTLE (16729-184-17)
Marketing
Marketing Status
Brand
hydrochlorothiazide
Generic
hydrochlorothiazide
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4b95022b-87b4-60ac-e063-6294a90afa9b", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH"], "rxcui": ["197770", "310798", "429503"], "spl_set_id": ["babb1b20-fe82-40ba-8e7a-0c56fe433b4a"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Accord Healthcare Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (16729-184-01)", "package_ndc": "16729-184-01", "marketing_start_date": "20130426"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (16729-184-17)", "package_ndc": "16729-184-17", "marketing_start_date": "20130410"}], "brand_name": "Hydrochlorothiazide", "product_id": "16729-184_4b95022b-87b4-60ac-e063-6294a90afa9b", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "16729-184", "generic_name": "Hydrochlorothiazide", "labeler_name": "Accord Healthcare Inc.", "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": "20271231"}