Package 0220-2155-41

Brand: fraxinus americana

Generic: fraxinus americana bark
NDC Package

Package Facts

Identity

Package NDC 0220-2155-41
Digits Only 0220215541
Product NDC 0220-2155
Description

6 [hp_C] in 1 TUBE (0220-2155-41)

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": "0a0ce402-1805-62f2-e063-6294a90a9770", "openfda": {"unii": ["0B24UR1O1S"], "spl_set_id": ["7acc5363-3280-1382-e053-2a91aa0aee02"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 [hp_C] in 1 TUBE (0220-2155-41)", "package_ndc": "0220-2155-41", "marketing_start_date": "19830303"}], "brand_name": "Fraxinus americana", "product_id": "0220-2155_0a0ce402-1805-62f2-e063-6294a90a9770", "dosage_form": "PELLET", "product_ndc": "0220-2155", "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": "6 [hp_C]/6[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}