Package 0220-2450-41
Brand: helleborus niger
Generic: helleborus niger rootPackage Facts
Identity
Package NDC
0220-2450-41
Digits Only
0220245041
Product NDC
0220-2450
Description
200 [kp_C] in 1 TUBE (0220-2450-41)
Marketing
Marketing Status
Brand
helleborus niger
Generic
helleborus niger root
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "003a848f-c8d0-0cb1-e063-6294a90a6602", "openfda": {"unii": ["608DGJ6815"], "spl_set_id": ["85b5c79a-5177-e5c0-e053-2991aa0a6ca3"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-2450-41)", "package_ndc": "0220-2450-41", "marketing_start_date": "19830303"}], "brand_name": "Helleborus niger", "product_id": "0220-2450_003a848f-c8d0-0cb1-e063-6294a90a6602", "dosage_form": "PELLET", "product_ndc": "0220-2450", "generic_name": "HELLEBORUS NIGER ROOT", "labeler_name": "Boiron", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Helleborus niger", "active_ingredients": [{"name": "HELLEBORUS NIGER ROOT", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}