Package 16571-888-06

Brand: nitrofurantoin

Generic: nitrofurantoin
NDC Package

Package Facts

Identity

Package NDC 16571-888-06
Digits Only 1657188806
Product NDC 16571-888
Description

1 BOTTLE in 1 CARTON (16571-888-06) / 60 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2024-02-01
Brand nitrofurantoin
Generic nitrofurantoin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b6694787-d7b8-4bcb-8dff-5ff30a83443a", "openfda": {"nui": ["N0000175494", "M0014892"], "unii": ["927AH8112L"], "rxcui": ["311989", "422434"], "spl_set_id": ["89095f4d-e142-465e-b378-da24f6eeaf2b"], "pharm_class_cs": ["Nitrofurans [CS]"], "pharm_class_epc": ["Nitrofuran Antibacterial [EPC]"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (16571-888-06)  / 60 mL in 1 BOTTLE", "package_ndc": "16571-888-06", "marketing_start_date": "20240201"}], "brand_name": "Nitrofurantoin", "product_id": "16571-888_b6694787-d7b8-4bcb-8dff-5ff30a83443a", "dosage_form": "SUSPENSION", "pharm_class": ["Nitrofuran Antibacterial [EPC]", "Nitrofurans [CS]"], "product_ndc": "16571-888", "generic_name": "Nitrofurantoin", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nitrofurantoin", "active_ingredients": [{"name": "NITROFURANTOIN", "strength": "50 mg/5mL"}], "application_number": "NDA009175", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20240201", "listing_expiration_date": "20261231"}