Package 68071-3608-3

Brand: hydrochlorothiazide

Generic: hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 68071-3608-3
Digits Only 6807136083
Product NDC 68071-3608
Description

30 TABLET in 1 BOTTLE, PLASTIC (68071-3608-3)

Marketing

Marketing Status
Marketed Since 2024-05-15
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": "1884e232-bf45-68a9-e063-6394a90a87a9", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0368071360837"], "unii": ["0J48LPH2TH"], "rxcui": ["429503"], "spl_set_id": ["1884db5f-72b5-6b0c-e063-6394a90a0e49"], "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, PLASTIC (68071-3608-3)", "package_ndc": "68071-3608-3", "marketing_start_date": "20240515"}], "brand_name": "HYDROCHLOROTHIAZIDE", "product_id": "68071-3608_1884e232-bf45-68a9-e063-6394a90a87a9", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "68071-3608", "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"}