Package 62135-738-90

Brand: hydrochlorothiazide

Generic: hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 62135-738-90
Digits Only 6213573890
Product NDC 62135-738
Product ID 62135-738_459c0f0e-ee69-96b0-e063-6294a90a03a1
Description

90 TABLET in 1 BOTTLE (62135-738-90)

Marketing

Marketing Status
Marketed Since 2023-07-28
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": "459c0f0e-ee69-96b0-e063-6294a90a03a1", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0362135449902", "0362135448059", "0362135448905", "0362135738907", "0362135449056"], "unii": ["0J48LPH2TH"], "rxcui": ["197770", "310798", "429503"], "spl_set_id": ["4e43dd27-3f4b-4205-a26e-6ecaa8281347"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (62135-738-90)", "package_ndc": "62135-738-90", "marketing_start_date": "20230728"}], "brand_name": "Hydrochlorothiazide", "product_id": "62135-738_459c0f0e-ee69-96b0-e063-6294a90a03a1", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "62135-738", "generic_name": "Hydrochlorothiazide", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}], "application_number": "ANDA085182", "marketing_category": "ANDA", "marketing_start_date": "20230502", "listing_expiration_date": "20261231"}