Package 0591-0347-01

Brand: hydrochlorothiazide

Generic: hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 0591-0347-01
Digits Only 0591034701
Product NDC 0591-0347
Description

100 CAPSULE, GELATIN COATED in 1 BOTTLE (0591-0347-01)

Marketing

Marketing Status
Marketed Since 1996-12-27
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": "b062bc7e-af92-4648-aed1-e02568313e21", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH"], "rxcui": ["199903"], "spl_set_id": ["a3eb7294-f913-434b-896c-da028bfebc73"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, GELATIN COATED in 1 BOTTLE (0591-0347-01)", "package_ndc": "0591-0347-01", "marketing_start_date": "19961227"}, {"sample": false, "description": "500 CAPSULE, GELATIN COATED in 1 BOTTLE (0591-0347-05)", "package_ndc": "0591-0347-05", "marketing_start_date": "19961227"}], "brand_name": "Hydrochlorothiazide", "product_id": "0591-0347_b062bc7e-af92-4648-aed1-e02568313e21", "dosage_form": "CAPSULE, GELATIN COATED", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "0591-0347", "generic_name": "Hydrochlorothiazide", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}], "application_number": "NDA020504", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "19961227", "listing_expiration_date": "20261231"}