Package 72603-176-01
Brand: nitrofurantoin
Generic: nitrofurantoinPackage Facts
Identity
Package NDC
72603-176-01
Digits Only
7260317601
Product NDC
72603-176
Description
1 BOTTLE in 1 CARTON (72603-176-01) / 230 mL in 1 BOTTLE
Marketing
Marketing Status
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": "14c9efac-c0b1-7afe-e063-6294a90a39e4", "openfda": {"nui": ["N0000175494", "M0014892"], "unii": ["927AH8112L"], "rxcui": ["311989"], "spl_set_id": ["04af8b73-7e15-7da8-e063-6294a90af284"], "pharm_class_cs": ["Nitrofurans [CS]"], "pharm_class_epc": ["Nitrofuran Antibacterial [EPC]"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (72603-176-01) / 230 mL in 1 BOTTLE", "package_ndc": "72603-176-01", "marketing_start_date": "20230417"}], "brand_name": "Nitrofurantoin", "product_id": "72603-176_14c9efac-c0b1-7afe-e063-6294a90a39e4", "dosage_form": "SUSPENSION", "pharm_class": ["Nitrofuran Antibacterial [EPC]", "Nitrofurans [CS]"], "product_ndc": "72603-176", "generic_name": "Nitrofurantoin", "labeler_name": "NorthStar Rx LLC", "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"}