Package 78670-150-01

Brand: iwilfin

Generic: eflornithine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 78670-150-01
Digits Only 7867015001
Product NDC 78670-150
Product ID 78670-150_49c998c7-d0b4-4527-8e34-dc5edc59a40f
Description

1 BOTTLE in 1 CARTON (78670-150-01) / 100 TABLET in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2024-01-15
Brand iwilfin
Generic eflornithine hydrochloride
Sample Package No

Linked Drug Pages (1)

iwilfin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "49c998c7-d0b4-4527-8e34-dc5edc59a40f", "openfda": {"unii": ["4NH22NDW9H"], "rxcui": ["2673199", "2673205"], "spl_set_id": ["6716d8cc-66e6-4cee-935c-ccb85ed984f5"], "manufacturer_name": ["USWM, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (78670-150-01)  / 100 TABLET in 1 BOTTLE", "package_ndc": "78670-150-01", "marketing_start_date": "20240115"}], "brand_name": "iwilfin", "product_id": "78670-150_49c998c7-d0b4-4527-8e34-dc5edc59a40f", "dosage_form": "TABLET", "pharm_class": ["Antiprotozoal [EPC]", "Decarboxylase Inhibitor [EPC]", "Decarboxylase Inhibitors [MoA]"], "product_ndc": "78670-150", "generic_name": "EFLORNITHINE HYDROCHLORIDE", "labeler_name": "USWM, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "iwilfin", "active_ingredients": [{"name": "EFLORNITHINE HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "NDA215500", "marketing_category": "NDA", "marketing_start_date": "20240115", "listing_expiration_date": "20261231"}