Package 0220-0230-41

Brand: ambrosia artemisiaefolia

Generic: ambrosia artemisiifolia
NDC Package

Package Facts

Identity

Package NDC 0220-0230-41
Digits Only 0220023041
Product NDC 0220-0230
Product ID 0220-0230_0c069179-fc7d-cf6b-e063-6394a90aeaeb
Description

200 [kp_C] in 1 TUBE (0220-0230-41)

Marketing

Marketing Status
Marketed Since 2024-01-01
Brand ambrosia artemisiaefolia
Generic ambrosia artemisiifolia
Sample Package No

Linked Drug Pages (1)

AMBROSIA ARTEMISIAEFOLIA ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0c069179-fc7d-cf6b-e063-6394a90aeaeb", "openfda": {"unii": ["9W34L2CQ9A"], "spl_set_id": ["0c069179-fc7c-cf6b-e063-6394a90aeaeb"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-0230-41)", "package_ndc": "0220-0230-41", "marketing_start_date": "20240101"}], "brand_name": "AMBROSIA ARTEMISIAEFOLIA", "product_id": "0220-0230_0c069179-fc7d-cf6b-e063-6394a90aeaeb", "dosage_form": "PELLET", "product_ndc": "0220-0230", "generic_name": "AMBROSIA ARTEMISIIFOLIA", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "AMBROSIA ARTEMISIAEFOLIA", "active_ingredients": [{"name": "AMBROSIA ARTEMISIIFOLIA", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20240101", "listing_expiration_date": "20261231"}