Package 70954-496-10

Brand: nitrofurantoin

Generic: nitrofurantoin
NDC Package

Package Facts

Identity

Package NDC 70954-496-10
Digits Only 7095449610
Product NDC 70954-496
Product ID 70954-496_7e94d701-0d57-4a04-bc74-d07febb8ad7b
Description

230 mL in 1 BOTTLE (70954-496-10)

Marketing

Marketing Status
Marketed Since 2023-04-17
Brand nitrofurantoin
Generic nitrofurantoin
Sample Package No

Linked Drug Pages (1)

Nitrofurantoin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "7e94d701-0d57-4a04-bc74-d07febb8ad7b", "openfda": {"nui": ["N0000175494", "M0014892"], "unii": ["927AH8112L"], "rxcui": ["311989"], "spl_set_id": ["3b377aff-2d4b-43ea-84c9-8e72c1421b7b"], "pharm_class_cs": ["Nitrofurans [CS]"], "pharm_class_epc": ["Nitrofuran Antibacterial [EPC]"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "230 mL in 1 BOTTLE (70954-496-10)", "package_ndc": "70954-496-10", "marketing_start_date": "20230417"}], "brand_name": "Nitrofurantoin", "product_id": "70954-496_7e94d701-0d57-4a04-bc74-d07febb8ad7b", "dosage_form": "SUSPENSION", "pharm_class": ["Nitrofuran Antibacterial [EPC]", "Nitrofurans [CS]"], "product_ndc": "70954-496", "generic_name": "Nitrofurantoin", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nitrofurantoin", "active_ingredients": [{"name": "NITROFURANTOIN", "strength": "25 mg/5mL"}], "application_number": "ANDA216385", "marketing_category": "ANDA", "marketing_start_date": "20230417", "listing_expiration_date": "20261231"}