Package 13668-676-30

Brand: dichlorphenamide

Generic: dichlorphenamide
NDC Package

Package Facts

Identity

Package NDC 13668-676-30
Digits Only 1366867630
Product NDC 13668-676
Description

30 TABLET in 1 BOTTLE (13668-676-30)

Marketing

Marketing Status
Marketed Since 2022-12-29
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": "1d0520f1-bf08-4def-a715-2ab45a18393e", "openfda": {"nui": ["N0000175517", "N0000000235", "M0020790"], "upc": ["0313668676303"], "unii": ["VVJ6673MHY"], "rxcui": ["197594"], "spl_set_id": ["64bf0c71-2113-47dc-8ce5-7fe535e558dc"], "pharm_class_cs": ["Sulfonamides [CS]"], "pharm_class_epc": ["Carbonic Anhydrase Inhibitor [EPC]"], "pharm_class_moa": ["Carbonic Anhydrase Inhibitors [MoA]"], "manufacturer_name": ["Torrent pharmaceuticals limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (13668-676-01)", "package_ndc": "13668-676-01", "marketing_start_date": "20221229"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (13668-676-30)", "package_ndc": "13668-676-30", "marketing_start_date": "20221229"}], "brand_name": "Dichlorphenamide", "product_id": "13668-676_1d0520f1-bf08-4def-a715-2ab45a18393e", "dosage_form": "TABLET", "pharm_class": ["Carbonic Anhydrase Inhibitor [EPC]", "Carbonic Anhydrase Inhibitors [MoA]", "Sulfonamides [CS]"], "product_ndc": "13668-676", "generic_name": "Dichlorphenamide", "labeler_name": "Torrent pharmaceuticals limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dichlorphenamide", "active_ingredients": [{"name": "DICHLORPHENAMIDE", "strength": "50 mg/1"}], "application_number": "ANDA215924", "marketing_category": "ANDA", "marketing_start_date": "20221229", "listing_expiration_date": "20271231"}