Package 0220-5259-41
Brand: viburnum opulus
Generic: viburnum opulus barkPackage Facts
Identity
Package NDC
0220-5259-41
Digits Only
0220525941
Product NDC
0220-5259
Description
9 [hp_C] in 1 TUBE (0220-5259-41)
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": "0a36799d-2e56-3100-e063-6294a90adf85", "openfda": {"unii": ["T1UG6H6805"], "spl_set_id": ["85dbe7ce-995a-21a8-e053-2a91aa0a4098"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "9 [hp_C] in 1 TUBE (0220-5259-41)", "package_ndc": "0220-5259-41", "marketing_start_date": "19830303"}], "brand_name": "VIBURNUM OPULUS", "product_id": "0220-5259_0a36799d-2e56-3100-e063-6294a90adf85", "dosage_form": "PELLET", "product_ndc": "0220-5259", "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": "9 [hp_C]/9[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}