Package 72789-381-90

Brand: hydrochlorothiazide

Generic: hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 72789-381-90
Digits Only 7278938190
Product NDC 72789-381
Product ID 72789-381_401ffc01-0f50-759c-e063-6394a90aa991
Description

90 TABLET in 1 BOTTLE, PLASTIC (72789-381-90)

Marketing

Marketing Status
Marketed Since 2024-02-20
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": "401ffc01-0f50-759c-e063-6394a90aa991", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0372789381909"], "unii": ["0J48LPH2TH"], "rxcui": ["310798"], "spl_set_id": ["1dc47186-3ecf-456f-b6d6-ba0f75c2504b"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (72789-381-90)", "package_ndc": "72789-381-90", "marketing_start_date": "20240220"}], "brand_name": "Hydrochlorothiazide", "product_id": "72789-381_401ffc01-0f50-759c-e063-6394a90aa991", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "72789-381", "generic_name": "Hydrochlorothiazide", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}], "application_number": "ANDA087059", "marketing_category": "ANDA", "marketing_start_date": "20200925", "listing_expiration_date": "20261231"}