Package 0220-5010-41

Brand: thuja occidentalis

Generic: thuja occidentalis leafy twig
NDC Package

Package Facts

Identity

Package NDC 0220-5010-41
Digits Only 0220501041
Product NDC 0220-5010
Product ID 0220-5010_445dbfa0-5464-e1d8-e063-6394a90a43be
Description

30 [hp_C] in 1 TUBE (0220-5010-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand thuja occidentalis
Generic thuja occidentalis leafy twig
Sample Package No

Linked Drug Pages (1)

Thuja occidentalis ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "445dbfa0-5464-e1d8-e063-6394a90a43be", "openfda": {"unii": ["1NT28V9397"], "spl_set_id": ["8635be15-68dc-777d-e053-2991aa0a193f"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_C] in 1 TUBE (0220-5010-41)", "package_ndc": "0220-5010-41", "marketing_start_date": "19830303"}], "brand_name": "Thuja occidentalis", "product_id": "0220-5010_445dbfa0-5464-e1d8-e063-6394a90a43be", "dosage_form": "PELLET", "product_ndc": "0220-5010", "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": "30 [hp_C]/30[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}