Package 0220-1841-41
Brand: echinacea angustifolia
Generic: echinacea angustifoliaPackage Facts
Identity
Package NDC
0220-1841-41
Digits Only
0220184141
Product NDC
0220-1841
Description
6 [hp_C] in 1 TUBE (0220-1841-41)
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-c4fc-ab5b-e063-6394a90ab630", "openfda": {"unii": ["VB06AV5US8"], "spl_set_id": ["858ecfc2-3690-0b5c-e053-2991aa0a1501"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 [hp_C] in 1 TUBE (0220-1841-41)", "package_ndc": "0220-1841-41", "marketing_start_date": "19830303"}], "brand_name": "Echinacea angustifolia", "product_id": "0220-1841_0a0ca58e-c4fc-ab5b-e063-6394a90ab630", "dosage_form": "PELLET", "product_ndc": "0220-1841", "generic_name": "ECHINACEA ANGUSTIFOLIA", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Echinacea angustifolia", "active_ingredients": [{"name": "ECHINACEA ANGUSTIFOLIA", "strength": "6 [hp_C]/6[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}