Package 68645-510-54

Brand: hydrochlorothiazide

Generic: hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 68645-510-54
Digits Only 6864551054
Product NDC 68645-510
Product ID 68645-510_4c4a2035-8173-6708-e063-6294a90ad6f2
Description

30 TABLET in 1 BOTTLE (68645-510-54)

Marketing

Marketing Status
Marketed Since 1973-01-12
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": "4c4a2035-8173-6708-e063-6294a90ad6f2", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0368645510545"], "unii": ["0J48LPH2TH"], "rxcui": ["310798"], "spl_set_id": ["1d6ea4b4-1e3c-4f3f-989c-1a3a3c0da6bd"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Legacy Pharmaceutical Packaging, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68645-510-54)", "package_ndc": "68645-510-54", "marketing_start_date": "19730112"}], "brand_name": "Hydrochlorothiazide", "product_id": "68645-510_4c4a2035-8173-6708-e063-6294a90ad6f2", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "68645-510", "generic_name": "Hydrochlorothiazide", "labeler_name": "Legacy Pharmaceutical Packaging, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}], "application_number": "ANDA083177", "marketing_category": "ANDA", "marketing_start_date": "19730112", "listing_expiration_date": "20271231"}