Package 0220-0844-41
Brand: berberis vulgaris
Generic: berberis vulgaris root barkPackage Facts
Identity
Package NDC
0220-0844-41
Digits Only
0220084441
Product NDC
0220-0844
Description
6 [hp_X] in 1 TUBE (0220-0844-41)
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": "09bab3c8-75c0-db5a-e063-6294a90a6d9c", "openfda": {"unii": ["1TH8Q20J0U"], "spl_set_id": ["8500d840-0c7a-3a6a-e053-2a91aa0ab1cd"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 [hp_X] in 1 TUBE (0220-0844-41)", "package_ndc": "0220-0844-41", "marketing_start_date": "19830303"}], "brand_name": "Berberis vulgaris", "product_id": "0220-0844_09bab3c8-75c0-db5a-e063-6294a90a6d9c", "dosage_form": "PELLET", "product_ndc": "0220-0844", "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_X]/6[hp_X]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}