Package 0220-0833-41
Brand: berberis vulgaris
Generic: berberis vulgaris root barkPackage Facts
Identity
Package NDC
0220-0833-41
Digits Only
0220083341
Product NDC
0220-0833
Description
12 [hp_C] in 1 TUBE (0220-0833-41)
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": "09bab5f5-59d9-5c85-e063-6394a90a7848", "openfda": {"unii": ["1TH8Q20J0U"], "spl_set_id": ["8478b671-deee-e992-e053-2a91aa0abb9e"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 [hp_C] in 1 TUBE (0220-0833-41)", "package_ndc": "0220-0833-41", "marketing_start_date": "19830303"}], "brand_name": "Berberis vulgaris", "product_id": "0220-0833_09bab5f5-59d9-5c85-e063-6394a90a7848", "dosage_form": "PELLET", "product_ndc": "0220-0833", "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": "12 [hp_C]/12[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}