Package 59651-206-23

Brand: nitrofurantoin

Generic: nitrofurantoin
NDC Package

Package Facts

Identity

Package NDC 59651-206-23
Digits Only 5965120623
Product NDC 59651-206
Product ID 59651-206_30c5502b-09bd-4fd7-bec8-aba74d302e09
Description

1 BOTTLE in 1 CARTON (59651-206-23) / 230 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2023-05-11
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": "30c5502b-09bd-4fd7-bec8-aba74d302e09", "openfda": {"upc": ["0359651206232"], "unii": ["E1QI2CQQ1I"], "spl_set_id": ["e9d10eaa-cf9c-469e-82ef-5af7285f2c86"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (59651-206-23)  / 230 mL in 1 BOTTLE", "package_ndc": "59651-206-23", "marketing_start_date": "20230511"}], "brand_name": "Nitrofurantoin", "product_id": "59651-206_30c5502b-09bd-4fd7-bec8-aba74d302e09", "dosage_form": "SUSPENSION", "pharm_class": ["Nitrofuran Antibacterial [EPC]", "Nitrofurans [CS]"], "product_ndc": "59651-206", "generic_name": "Nitrofurantoin", "labeler_name": "Aurobindo Pharma Limited", "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"}