Package 51655-422-52

Brand: hydrochlorothiazide

Generic: hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 51655-422-52
Digits Only 5165542252
Product NDC 51655-422
Product ID 51655-422_49ecc98b-83c6-d23d-e063-6394a90a30bc
Description

30 TABLET in 1 BOTTLE, PLASTIC (51655-422-52)

Marketing

Marketing Status
Marketed Since 2023-06-06
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": "49ecc98b-83c6-d23d-e063-6394a90a30bc", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH"], "rxcui": ["197770"], "spl_set_id": ["f2f3b60a-bffe-2675-e053-2995a90ae96e"], "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 (51655-422-26)", "package_ndc": "51655-422-26", "marketing_start_date": "20221229"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-422-52)", "package_ndc": "51655-422-52", "marketing_start_date": "20230606"}], "brand_name": "Hydrochlorothiazide", "product_id": "51655-422_49ecc98b-83c6-d23d-e063-6394a90a30bc", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "51655-422", "generic_name": "Hydrochlorothiazide", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "50 mg/1"}], "application_number": "ANDA040907", "marketing_category": "ANDA", "marketing_start_date": "20221229", "listing_expiration_date": "20271231"}