Package 72789-296-30
Brand: hydrochlorothiazide
Generic: hydrochlorothiazidePackage Facts
Identity
Package NDC
72789-296-30
Digits Only
7278929630
Product NDC
72789-296
Description
30 TABLET in 1 BOTTLE, PLASTIC (72789-296-30)
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": "401f4a29-5b2a-ab5a-e063-6394a90afd66", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0372789296302"], "unii": ["0J48LPH2TH"], "rxcui": ["310798"], "spl_set_id": ["89d367b1-de04-4970-9967-27a1c7711c0f"], "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": "30 TABLET in 1 BOTTLE, PLASTIC (72789-296-30)", "package_ndc": "72789-296-30", "marketing_start_date": "20221230"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (72789-296-60)", "package_ndc": "72789-296-60", "marketing_start_date": "20230727"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (72789-296-90)", "package_ndc": "72789-296-90", "marketing_start_date": "20221228"}], "brand_name": "Hydrochlorothiazide", "product_id": "72789-296_401f4a29-5b2a-ab5a-e063-6394a90afd66", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "72789-296", "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"}