Package 71610-021-09

Brand: chlorthalidone

Generic: chlorthalidone
NDC Package

Package Facts

Identity

Package NDC 71610-021-09
Digits Only 7161002109
Product NDC 71610-021
Description

9000 TABLET in 1 BOTTLE (71610-021-09)

Marketing

Marketing Status
Marketed Since 2017-12-20
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": "6d839289-f4c6-44d7-a6f5-a4c178766fb2", "openfda": {"nui": ["N0000175359", "N0000175420"], "unii": ["Q0MQD1073Q"], "rxcui": ["197500"], "spl_set_id": ["5ea42479-84f4-434d-b65b-de34a7a57926"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide-like Diuretic [EPC]"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "9000 TABLET in 1 BOTTLE (71610-021-09)", "package_ndc": "71610-021-09", "marketing_start_date": "20171220"}], "brand_name": "Chlorthalidone", "product_id": "71610-021_6d839289-f4c6-44d7-a6f5-a4c178766fb2", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide-like Diuretic [EPC]"], "product_ndc": "71610-021", "generic_name": "Chlorthalidone", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorthalidone", "active_ingredients": [{"name": "CHLORTHALIDONE", "strength": "50 mg/1"}], "application_number": "ANDA089286", "marketing_category": "ANDA", "marketing_start_date": "20160212", "listing_expiration_date": "20261231"}