Package 63629-1218-1

Brand: hydrochlorothiazide

Generic: hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 63629-1218-1
Digits Only 6362912181
Product NDC 63629-1218
Description

100 TABLET in 1 BOTTLE (63629-1218-1)

Marketing

Marketing Status
Marketed Since 2021-01-14
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": "2aa1f09a-0647-47d1-8191-bafbd148771a", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH"], "rxcui": ["310798"], "spl_set_id": ["5f2e72cc-073d-4bb5-95fe-53d4060127ec"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (63629-1218-1)", "package_ndc": "63629-1218-1", "marketing_start_date": "20210114"}], "brand_name": "Hydrochlorothiazide", "product_id": "63629-1218_2aa1f09a-0647-47d1-8191-bafbd148771a", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "63629-1218", "generic_name": "Hydrochlorothiazide", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}], "application_number": "ANDA040412", "marketing_category": "ANDA", "marketing_start_date": "20020329", "listing_expiration_date": "20261231"}