Package 53645-1220-2

Brand: thuja

Generic: thuja
NDC Package

Package 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
Marketed Since 2013-06-21
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"}