Package 68071-3652-1

Brand: hydrochlorothiazide

Generic: hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 68071-3652-1
Digits Only 6807136521
Product NDC 68071-3652
Product ID 68071-3652_1e028af3-119f-2ca1-e063-6294a90a68a0
Description

100 TABLET in 1 BOTTLE, PLASTIC (68071-3652-1)

Marketing

Marketing Status
Marketed Since 2024-07-24
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": "1e028af3-119f-2ca1-e063-6294a90a68a0", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0368071365214"], "unii": ["0J48LPH2TH"], "rxcui": ["429503"], "spl_set_id": ["1e02787f-ccb5-abc2-e063-6294a90af7c3"], "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": "100 TABLET in 1 BOTTLE, PLASTIC (68071-3652-1)", "package_ndc": "68071-3652-1", "marketing_start_date": "20240724"}], "brand_name": "HYDROCHLOROTHIAZIDE", "product_id": "68071-3652_1e028af3-119f-2ca1-e063-6294a90a68a0", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "68071-3652", "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": "ANDA040702", "marketing_category": "ANDA", "marketing_start_date": "20191101", "listing_expiration_date": "20261231"}