Package 51672-4237-4

Brand: deferiprone

Generic: deferiprone
NDC Package

Package Facts

Identity

Package NDC 51672-4237-4
Digits Only 5167242374
Product NDC 51672-4237
Product ID 51672-4237_3631d351-4653-3512-e063-6394a90a81c0
Description

50 TABLET in 1 BOTTLE (51672-4237-4)

Marketing

Marketing Status
Marketed Since 2024-02-05
Brand deferiprone
Generic deferiprone
Sample Package No

Linked Drug Pages (1)

Deferiprone ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3631d351-4653-3512-e063-6394a90a81c0", "openfda": {"nui": ["N0000000144", "N0000175522"], "unii": ["2BTY8KH53L"], "rxcui": ["389242", "2180997"], "spl_set_id": ["5af1643d-4c6e-4668-ae9b-1046f0ad6d8a"], "pharm_class_epc": ["Iron Chelator [EPC]"], "pharm_class_moa": ["Iron Chelating Activity [MoA]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET in 1 BOTTLE (51672-4237-4)", "package_ndc": "51672-4237-4", "marketing_start_date": "20240205"}], "brand_name": "Deferiprone", "product_id": "51672-4237_3631d351-4653-3512-e063-6394a90a81c0", "dosage_form": "TABLET", "pharm_class": ["Iron Chelating Activity [MoA]", "Iron Chelator [EPC]"], "product_ndc": "51672-4237", "generic_name": "Deferiprone", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Deferiprone", "active_ingredients": [{"name": "DEFERIPRONE", "strength": "1000 mg/1"}], "application_number": "ANDA208800", "marketing_category": "ANDA", "marketing_start_date": "20240205", "listing_expiration_date": "20261231"}