Package 0220-5258-41
Brand: viburnum opulus
Generic: viburnum opulus barkPackage Facts
Identity
Package NDC
0220-5258-41
Digits Only
0220525841
Product NDC
0220-5258
Description
5 [hp_C] in 1 TUBE (0220-5258-41)
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": "0a35ec95-6aa5-333e-e063-6394a90a4b1b", "openfda": {"unii": ["T1UG6H6805"], "spl_set_id": ["813fc42e-37f0-6530-e053-2991aa0ad80d"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 [hp_C] in 1 TUBE (0220-5258-41)", "package_ndc": "0220-5258-41", "marketing_start_date": "19830303"}], "brand_name": "Viburnum opulus", "product_id": "0220-5258_0a35ec95-6aa5-333e-e063-6394a90a4b1b", "dosage_form": "PELLET", "product_ndc": "0220-5258", "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": "5 [hp_C]/5[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}