Package 16571-242-01

Brand: dichlorphenamide

Generic: dichlorphenamide
NDC Package

Package Facts

Identity

Package NDC 16571-242-01
Digits Only 1657124201
Product NDC 16571-242
Description

100 TABLET in 1 BOTTLE (16571-242-01)

Marketing

Marketing Status
Marketed Since 2025-11-18
Brand dichlorphenamide
Generic dichlorphenamide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3ef66eca-f35a-46a8-bebe-b286dfbbb376", "openfda": {"nui": ["N0000175517", "N0000000235", "M0020790"], "upc": ["0316571242016"], "unii": ["VVJ6673MHY"], "rxcui": ["197594"], "spl_set_id": ["35b9c81a-5062-451d-8b0c-1b599113aa6c"], "pharm_class_cs": ["Sulfonamides [CS]"], "pharm_class_epc": ["Carbonic Anhydrase Inhibitor [EPC]"], "pharm_class_moa": ["Carbonic Anhydrase Inhibitors [MoA]"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (16571-242-01)", "package_ndc": "16571-242-01", "marketing_start_date": "20251118"}], "brand_name": "Dichlorphenamide", "product_id": "16571-242_3ef66eca-f35a-46a8-bebe-b286dfbbb376", "dosage_form": "TABLET", "pharm_class": ["Carbonic Anhydrase Inhibitor [EPC]", "Carbonic Anhydrase Inhibitors [MoA]", "Sulfonamides [CS]"], "product_ndc": "16571-242", "generic_name": "Dichlorphenamide", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dichlorphenamide", "active_ingredients": [{"name": "DICHLORPHENAMIDE", "strength": "50 mg/1"}], "application_number": "ANDA218783", "marketing_category": "ANDA", "marketing_start_date": "20251118", "listing_expiration_date": "20261231"}