Package 0220-0829-41
Brand: berberis vulgaris
Generic: berberis vulgaris root barkPackage Facts
Identity
Package NDC
0220-0829-41
Digits Only
0220082941
Product NDC
0220-0829
Description
6 [hp_C] in 1 TUBE (0220-0829-41)
Marketing
Marketing Status
Brand
berberis vulgaris
Generic
berberis vulgaris root bark
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "09bab28f-d72d-f2e7-e063-6294a90a1b79", "openfda": {"unii": ["1TH8Q20J0U"], "spl_set_id": ["847863e9-016c-09bf-e053-2991aa0ace76"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 [hp_C] in 1 TUBE (0220-0829-41)", "package_ndc": "0220-0829-41", "marketing_start_date": "19830303"}], "brand_name": "Berberis vulgaris", "product_id": "0220-0829_09bab28f-d72d-f2e7-e063-6294a90a1b79", "dosage_form": "PELLET", "product_ndc": "0220-0829", "generic_name": "BERBERIS VULGARIS ROOT BARK", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Berberis vulgaris", "active_ingredients": [{"name": "BERBERIS VULGARIS ROOT BARK", "strength": "6 [hp_C]/6[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}