Package 42708-079-30

Brand: hydrochlorothiazide

Generic: hydrochlorothiazide
NDC Package Sample

Package Facts

Identity

Package NDC 42708-079-30
Digits Only 4270807930
Product NDC 42708-079
Product ID 42708-079_46533783-5cb8-c0bd-e063-6294a90a8dd8
Description

30 TABLET in 1 BOTTLE (42708-079-30)

Marketing

Marketing Status
Marketed Since 2019-02-11
Brand hydrochlorothiazide
Generic hydrochlorothiazide
Sample Package Yes

Linked Drug Pages (1)

Hydrochlorothiazide ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "46533783-5cb8-c0bd-e063-6294a90a8dd8", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH"], "rxcui": ["310798"], "spl_set_id": ["9cd5d16e-3db7-4b25-847d-6de91543463b"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["QPharma, Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "30 TABLET in 1 BOTTLE (42708-079-30)", "package_ndc": "42708-079-30", "marketing_start_date": "20190211"}], "brand_name": "Hydrochlorothiazide", "product_id": "42708-079_46533783-5cb8-c0bd-e063-6294a90a8dd8", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "42708-079", "generic_name": "Hydrochlorothiazide", "labeler_name": "QPharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}], "application_number": "ANDA040907", "marketing_category": "ANDA", "marketing_start_date": "20080815", "listing_expiration_date": "20261231"}