Package 0220-1844-41
Brand: echinacea angustifolia
Generic: echinacea angustifoliaPackage Facts
Identity
Package NDC
0220-1844-41
Digits Only
0220184441
Product NDC
0220-1844
Description
30 [hp_C] in 1 TUBE (0220-1844-41)
Marketing
Marketing Status
Brand
echinacea angustifolia
Generic
echinacea angustifolia
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0a0ca58e-c4fd-ab5b-e063-6394a90ab630", "openfda": {"unii": ["VB06AV5US8"], "spl_set_id": ["858f626f-d3e2-89e6-e053-2991aa0a6349"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_C] in 1 TUBE (0220-1844-41)", "package_ndc": "0220-1844-41", "marketing_start_date": "19830303"}], "brand_name": "Echinacea angustifolia", "product_id": "0220-1844_0a0ca58e-c4fd-ab5b-e063-6394a90ab630", "dosage_form": "PELLET", "product_ndc": "0220-1844", "generic_name": "ECHINACEA ANGUSTIFOLIA", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Echinacea angustifolia", "active_ingredients": [{"name": "ECHINACEA ANGUSTIFOLIA", "strength": "30 [hp_C]/30[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}