Package 71335-2935-1

Brand: chlorthalidone

Generic: chlorthalidone
NDC Package

Package Facts

Identity

Package NDC 71335-2935-1
Digits Only 7133529351
Product NDC 71335-2935
Description

1000 TABLET in 1 BOTTLE (71335-2935-1)

Marketing

Marketing Status
Marketed Since 2025-10-28
Brand chlorthalidone
Generic chlorthalidone
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "bfae447d-61c7-47f6-b7d9-e972c7a7963c", "openfda": {"nui": ["N0000175359", "N0000175420"], "unii": ["Q0MQD1073Q"], "rxcui": ["197499"], "spl_set_id": ["d8373bde-c8c9-445a-8933-49394023414a"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide-like Diuretic [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (71335-2935-1)", "package_ndc": "71335-2935-1", "marketing_start_date": "20251028"}], "brand_name": "Chlorthalidone", "product_id": "71335-2935_bfae447d-61c7-47f6-b7d9-e972c7a7963c", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide-like Diuretic [EPC]"], "product_ndc": "71335-2935", "generic_name": "Chlorthalidone", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorthalidone", "active_ingredients": [{"name": "CHLORTHALIDONE", "strength": "25 mg/1"}], "application_number": "ANDA212878", "marketing_category": "ANDA", "marketing_start_date": "20220805", "listing_expiration_date": "20261231"}