Package 0220-9356-43

Brand: thuja occidentalis 30c

Generic: thuja occidentalis
NDC Package

Package Facts

Identity

Package NDC 0220-9356-43
Digits Only 0220935643
Product NDC 0220-9356
Description

30 [hp_C] in 1 PACKAGE (0220-9356-43)

Marketing

Marketing Status
Marketed Since 2017-03-15
Brand thuja occidentalis 30c
Generic thuja occidentalis
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "441fe92c-ce78-3112-e063-6394a90a7c97", "openfda": {"unii": ["1NT28V9397"], "spl_set_id": ["5e35616f-b057-0f18-e053-2991aa0a5749"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_C] in 1 PACKAGE (0220-9356-43)", "package_ndc": "0220-9356-43", "marketing_start_date": "20170315"}], "brand_name": "Thuja occidentalis 30C", "product_id": "0220-9356_441fe92c-ce78-3112-e063-6394a90a7c97", "dosage_form": "PELLET", "product_ndc": "0220-9356", "generic_name": "THUJA OCCIDENTALIS", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Thuja occidentalis 30C", "active_ingredients": [{"name": "THUJA OCCIDENTALIS LEAFY TWIG", "strength": "30 [hp_C]/30[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20170315", "listing_expiration_date": "20261231"}