Package 0220-0219-43

Brand: ambrosia artemisiaefolia

Generic: ambrosia artemisiifolia
NDC Package

Package Facts

Identity

Package NDC 0220-0219-43
Digits Only 0220021943
Product NDC 0220-0219
Product ID 0220-0219_10e04d03-329d-090f-e063-6294a90a6c72
Description

3 TUBE in 1 PACKAGE (0220-0219-43) / 30 [hp_C] in 1 TUBE

Marketing

Marketing Status
Marketed Since 2020-05-11
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": "10e04d03-329d-090f-e063-6294a90a6c72", "openfda": {"unii": ["9W34L2CQ9A"], "spl_set_id": ["8427717f-4d1a-54b5-e053-2a91aa0a3d00"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_C] in 1 TUBE (0220-0219-41)", "package_ndc": "0220-0219-41", "marketing_start_date": "19830303"}, {"sample": false, "description": "3 TUBE in 1 PACKAGE (0220-0219-43)  / 30 [hp_C] in 1 TUBE", "package_ndc": "0220-0219-43", "marketing_start_date": "20200511"}], "brand_name": "Ambrosia artemisiaefolia", "product_id": "0220-0219_10e04d03-329d-090f-e063-6294a90a6c72", "dosage_form": "PELLET", "product_ndc": "0220-0219", "generic_name": "AMBROSIA ARTEMISIIFOLIA", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ambrosia artemisiaefolia", "active_ingredients": [{"name": "AMBROSIA ARTEMISIIFOLIA", "strength": "30 [hp_C]/30[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}