Package 13517-135-06

Brand: nitazoxanide

Generic: nitazoxanide
NDC Package

Package Facts

Identity

Package NDC 13517-135-06
Digits Only 1351713506
Product NDC 13517-135
Product ID 13517-135_db1d15c7-d9af-410f-98d5-bd6e8f84c815
Description

6 TABLET in 1 BOTTLE (13517-135-06)

Marketing

Marketing Status
Marketed Since 2026-01-26
Brand nitazoxanide
Generic nitazoxanide
Sample Package No

Linked Drug Pages (1)

Nitazoxanide ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "db1d15c7-d9af-410f-98d5-bd6e8f84c815", "openfda": {"nui": ["N0000175485"], "upc": ["0313517135067"], "unii": ["SOA12P041N"], "rxcui": ["427163"], "spl_set_id": ["40a7cc30-76cd-49fe-965a-7823c4140d0f"], "pharm_class_epc": ["Antiprotozoal [EPC]"], "manufacturer_name": ["e5 Pharma, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET in 1 BOTTLE (13517-135-06)", "package_ndc": "13517-135-06", "marketing_start_date": "20260126"}], "brand_name": "Nitazoxanide", "product_id": "13517-135_db1d15c7-d9af-410f-98d5-bd6e8f84c815", "dosage_form": "TABLET", "pharm_class": ["Antiprotozoal [EPC]"], "product_ndc": "13517-135", "generic_name": "Nitazoxanide", "labeler_name": "e5 Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nitazoxanide", "active_ingredients": [{"name": "NITAZOXANIDE", "strength": "500 mg/1"}], "application_number": "ANDA214844", "marketing_category": "ANDA", "marketing_start_date": "20260126", "listing_expiration_date": "20271231"}