Package 0220-5013-41
Brand: thuja occidentalis
Generic: thuja occidentalis leafy twigPackage Facts
Identity
Package NDC
0220-5013-41
Digits Only
0220501341
Product NDC
0220-5013
Description
12 [hp_X] in 1 TUBE (0220-5013-41)
Marketing
Marketing Status
Brand
thuja occidentalis
Generic
thuja occidentalis leafy twig
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "445d6a23-c9df-8cff-e063-6294a90ad219", "openfda": {"unii": ["1NT28V9397"], "spl_set_id": ["8634df03-1d21-152d-e053-2991aa0ab3a7"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 [hp_X] in 1 TUBE (0220-5013-41)", "package_ndc": "0220-5013-41", "marketing_start_date": "19830303"}], "brand_name": "Thuja occidentalis", "product_id": "0220-5013_445d6a23-c9df-8cff-e063-6294a90ad219", "dosage_form": "PELLET", "product_ndc": "0220-5013", "generic_name": "THUJA OCCIDENTALIS LEAFY TWIG", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Thuja occidentalis", "active_ingredients": [{"name": "THUJA OCCIDENTALIS LEAFY TWIG", "strength": "12 [hp_X]/12[hp_X]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}