Package 53645-1220-2
Brand: thuja
Generic: thujaPackage Facts
Identity
Package NDC
53645-1220-2
Digits Only
5364512202
Product NDC
53645-1220
Description
23 g in 1 BOTTLE (53645-1220-2)
Marketing
Marketing Status
Brand
thuja
Generic
thuja
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b99bad22-372f-22f5-e053-2995a90a70f0", "openfda": {"unii": ["1NT28V9397"], "spl_set_id": ["34dea719-92b7-4b90-96fe-5270403e9b95"], "manufacturer_name": ["True Botanica, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "23 g in 1 BOTTLE (53645-1220-2)", "package_ndc": "53645-1220-2", "marketing_start_date": "20130621"}], "brand_name": "Thuja", "product_id": "53645-1220_b99bad22-372f-22f5-e053-2995a90a70f0", "dosage_form": "GLOBULE", "product_ndc": "53645-1220", "generic_name": "Thuja", "labeler_name": "True Botanica, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Thuja", "active_ingredients": [{"name": "THUJA OCCIDENTALIS LEAFY TWIG", "strength": "6 [hp_X]/23g"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20130621", "listing_expiration_date": "20261231"}