Package 0220-0218-41

Brand: ambrosia artemisiaefolia

Generic: ambrosia artemisiifolia
NDC Package

Package Facts

Identity

Package NDC 0220-0218-41
Digits Only 0220021841
Product NDC 0220-0218
Product ID 0220-0218_10e1b09c-a346-f74f-e063-6394a90a3b7c
Description

6 [hp_C] in 1 TUBE (0220-0218-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
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": "10e1b09c-a346-f74f-e063-6394a90a3b7c", "openfda": {"unii": ["9W34L2CQ9A"], "spl_set_id": ["8427439b-f497-5dd7-e053-2991aa0a591b"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 [hp_C] in 1 TUBE (0220-0218-41)", "package_ndc": "0220-0218-41", "marketing_start_date": "19830303"}], "brand_name": "Ambrosia artemisiaefolia", "product_id": "0220-0218_10e1b09c-a346-f74f-e063-6394a90a3b7c", "dosage_form": "PELLET", "product_ndc": "0220-0218", "generic_name": "AMBROSIA ARTEMISIIFOLIA", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ambrosia artemisiaefolia", "active_ingredients": [{"name": "AMBROSIA ARTEMISIIFOLIA", "strength": "6 [hp_C]/6[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}