Package 51655-515-52
Brand: hydrochlorothiazide
Generic: hydrochlorothiazidePackage Facts
Identity
Package NDC
51655-515-52
Digits Only
5165551552
Product NDC
51655-515
Description
30 TABLET in 1 BOTTLE, PLASTIC (51655-515-52)
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": "490fa174-86ca-51ab-e063-6394a90a351f", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH"], "rxcui": ["310798"], "spl_set_id": ["f3191ca2-4dbc-01f5-e053-2a95a90a572c"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (51655-515-26)", "package_ndc": "51655-515-26", "marketing_start_date": "20220817"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-515-52)", "package_ndc": "51655-515-52", "marketing_start_date": "20221020"}], "brand_name": "Hydrochlorothiazide", "product_id": "51655-515_490fa174-86ca-51ab-e063-6394a90a351f", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "51655-515", "generic_name": "Hydrochlorothiazide", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}], "application_number": "ANDA202556", "marketing_category": "ANDA", "marketing_start_date": "20220817", "listing_expiration_date": "20271231"}