Package 0220-2156-41

Brand: fraxinus americana

Generic: fraxinus americana bark
NDC Package

Package Facts

Identity

Package NDC 0220-2156-41
Digits Only 0220215641
Product NDC 0220-2156
Description

30 [hp_C] in 1 TUBE (0220-2156-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand fraxinus americana
Generic fraxinus americana bark
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f52926bd-b7fb-8070-e053-2a95a90ac58d", "openfda": {"unii": ["0B24UR1O1S"], "spl_set_id": ["85a180d8-01c6-78b8-e053-2991aa0aed90"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_C] in 1 TUBE (0220-2156-41)", "package_ndc": "0220-2156-41", "marketing_start_date": "19830303"}], "brand_name": "Fraxinus americana", "product_id": "0220-2156_f52926bd-b7fb-8070-e053-2a95a90ac58d", "dosage_form": "PELLET", "product_ndc": "0220-2156", "generic_name": "FRAXINUS AMERICANA BARK", "labeler_name": "Boiron", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fraxinus americana", "active_ingredients": [{"name": "FRAXINUS AMERICANA BARK", "strength": "30 [hp_C]/30[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}