Package 0220-5004-41

Brand: thuja occidentalis

Generic: thuja occidentalis leafy twig
NDC Package

Package Facts

Identity

Package NDC 0220-5004-41
Digits Only 0220500441
Product NDC 0220-5004
Description

7 [hp_C] in 1 TUBE (0220-5004-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
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": "445ee5fe-9458-28aa-e063-6294a90a9570", "openfda": {"unii": ["1NT28V9397"], "spl_set_id": ["8641c09a-267e-2cda-e053-2991aa0a2cdf"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "7 [hp_C] in 1 TUBE (0220-5004-41)", "package_ndc": "0220-5004-41", "marketing_start_date": "19830303"}], "brand_name": "Thuja occidentalis", "product_id": "0220-5004_445ee5fe-9458-28aa-e063-6294a90a9570", "dosage_form": "PELLET", "product_ndc": "0220-5004", "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": "7 [hp_C]/7[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}