Package 64980-593-24

Brand: nitrofurantoin

Generic: nitrofurantoin
NDC Package

Package Facts

Identity

Package NDC 64980-593-24
Digits Only 6498059324
Product NDC 64980-593
Description

1 BOTTLE in 1 CARTON (64980-593-24) / 230 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2023-05-11
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": "dfecf83b-2b30-4505-9044-bec3dce43a39", "openfda": {"unii": ["E1QI2CQQ1I"], "rxcui": ["311989"], "spl_set_id": ["11e700aa-66f9-4939-8a6b-a23240ae1a0b"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (64980-593-24)  / 230 mL in 1 BOTTLE", "package_ndc": "64980-593-24", "marketing_start_date": "20230511"}], "brand_name": "Nitrofurantoin", "product_id": "64980-593_dfecf83b-2b30-4505-9044-bec3dce43a39", "dosage_form": "SUSPENSION", "pharm_class": ["Nitrofuran Antibacterial [EPC]", "Nitrofurans [CS]"], "product_ndc": "64980-593", "generic_name": "Nitrofurantoin", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nitrofurantoin", "active_ingredients": [{"name": "NITROFURANTOIN MONOHYDRATE", "strength": "25 mg/5mL"}], "application_number": "ANDA212607", "marketing_category": "ANDA", "marketing_start_date": "20230511", "listing_expiration_date": "20261231"}