Package 68071-3443-3

Brand: hydrochlorothiazide

Generic: hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 68071-3443-3
Digits Only 6807134433
Product NDC 68071-3443
Product ID 68071-3443_339e8633-2e2a-26d1-e063-6394a90aa72e
Description

30 TABLET in 1 BOTTLE (68071-3443-3)

Marketing

Marketing Status
Marketed Since 2023-06-21
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": "339e8633-2e2a-26d1-e063-6394a90aa72e", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0368071344332"], "unii": ["0J48LPH2TH"], "rxcui": ["429503"], "spl_set_id": ["fea5a353-9b13-9b87-e053-6394a90a627d"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-3443-3)", "package_ndc": "68071-3443-3", "marketing_start_date": "20230621"}], "brand_name": "Hydrochlorothiazide", "product_id": "68071-3443_339e8633-2e2a-26d1-e063-6394a90aa72e", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "68071-3443", "generic_name": "Hydrochlorothiazide", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}], "application_number": "ANDA040707", "marketing_category": "ANDA", "marketing_start_date": "20070312", "listing_expiration_date": "20261231"}