Package 0220-5255-41
Brand: viburnum opulus
Generic: viburnum opulus barkPackage Facts
Identity
Package NDC
0220-5255-41
Digits Only
0220525541
Product NDC
0220-5255
Description
200 [kp_C] in 1 TUBE (0220-5255-41)
Marketing
Marketing Status
Brand
viburnum opulus
Generic
viburnum opulus bark
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3a73d299-23a3-a3bf-e063-6394a90a6fea", "openfda": {"unii": ["T1UG6H6805"], "spl_set_id": ["3a73d299-23a2-a3bf-e063-6394a90a6fea"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-5255-41)", "package_ndc": "0220-5255-41", "marketing_start_date": "20250101"}], "brand_name": "VIBURNUM OPULUS", "product_id": "0220-5255_3a73d299-23a3-a3bf-e063-6394a90a6fea", "dosage_form": "PELLET", "product_ndc": "0220-5255", "generic_name": "VIBURNUM OPULUS BARK", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "VIBURNUM OPULUS", "active_ingredients": [{"name": "VIBURNUM OPULUS BARK", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20250101", "listing_expiration_date": "20261231"}