Package 71335-2914-1

Brand: nitrofurantoin

Generic: nitrofurantoin
NDC Package

Package Facts

Identity

Package NDC 71335-2914-1
Digits Only 7133529141
Product NDC 71335-2914
Description

100 CAPSULE in 1 BOTTLE (71335-2914-1)

Marketing

Marketing Status
Marketed Since 2025-10-22
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": "6818d7fb-4946-42bc-ade4-e9055846194b", "openfda": {"nui": ["N0000175494", "M0014892"], "unii": ["927AH8112L", "E1QI2CQQ1I"], "rxcui": ["1648755"], "spl_set_id": ["1c5db054-58af-4932-8fad-c3883b13f987"], "pharm_class_cs": ["Nitrofurans [CS]"], "pharm_class_epc": ["Nitrofuran Antibacterial [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (71335-2914-1)", "package_ndc": "71335-2914-1", "marketing_start_date": "20251022"}], "brand_name": "Nitrofurantoin", "product_id": "71335-2914_6818d7fb-4946-42bc-ade4-e9055846194b", "dosage_form": "CAPSULE", "pharm_class": ["Nitrofuran Antibacterial [EPC]", "Nitrofuran Antibacterial [EPC]", "Nitrofurans [CS]", "Nitrofurans [CS]"], "product_ndc": "71335-2914", "generic_name": "Nitrofurantoin", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nitrofurantoin", "active_ingredients": [{"name": "NITROFURANTOIN", "strength": "25 mg/1"}, {"name": "NITROFURANTOIN MONOHYDRATE", "strength": "75 mg/1"}], "application_number": "ANDA208516", "marketing_category": "ANDA", "marketing_start_date": "20180101", "listing_expiration_date": "20261231"}