Package 0220-2559-41

Brand: hydrastis canadensis

Generic: goldenseal
NDC Package

Package Facts

Identity

Package NDC 0220-2559-41
Digits Only 0220255941
Product NDC 0220-2559
Description

30 [hp_X] in 1 TUBE (0220-2559-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand hydrastis canadensis
Generic goldenseal
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f527e40a-56a0-3df5-e053-2a95a90a2dd7", "openfda": {"unii": ["ZW3Z11D0JV"], "spl_set_id": ["85ba819e-830f-0c84-e053-2991aa0a5118"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_X] in 1 TUBE (0220-2559-41)", "package_ndc": "0220-2559-41", "marketing_start_date": "19830303"}], "brand_name": "Hydrastis canadensis", "product_id": "0220-2559_f527e40a-56a0-3df5-e053-2a95a90a2dd7", "dosage_form": "PELLET", "product_ndc": "0220-2559", "generic_name": "GOLDENSEAL", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Hydrastis canadensis", "active_ingredients": [{"name": "GOLDENSEAL", "strength": "30 [hp_X]/30[hp_X]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}