Package 70954-934-10

Brand: nitazoxanide

Generic: nitazoxanide
NDC Package

Package Facts

Identity

Package NDC 70954-934-10
Digits Only 7095493410
Product NDC 70954-934
Product ID 70954-934_cd3652fa-a183-4fb6-9a21-73fbeba6fc4b
Description

6 TABLET in 1 BOTTLE (70954-934-10)

Marketing

Marketing Status
Marketed Since 2025-03-05
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": "cd3652fa-a183-4fb6-9a21-73fbeba6fc4b", "openfda": {"nui": ["N0000175485"], "upc": ["0370954934103"], "unii": ["SOA12P041N"], "rxcui": ["427163"], "spl_set_id": ["cd3652fa-a183-4fb6-9a21-73fbeba6fc4b"], "pharm_class_epc": ["Antiprotozoal [EPC]"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET in 1 BOTTLE (70954-934-10)", "package_ndc": "70954-934-10", "marketing_start_date": "20250305"}], "brand_name": "Nitazoxanide", "product_id": "70954-934_cd3652fa-a183-4fb6-9a21-73fbeba6fc4b", "dosage_form": "TABLET", "pharm_class": ["Antiprotozoal [EPC]"], "product_ndc": "70954-934", "generic_name": "Nitazoxanide", "labeler_name": "ANI Pharmaceuticals, Inc.", "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": "20250305", "listing_expiration_date": "20261231"}