Package 0220-5160-41
Brand: uva ursi
Generic: arctostaphylos uva ursi leafPackage Facts
Identity
Package NDC
0220-5160-41
Digits Only
0220516041
Product NDC
0220-5160
Description
8 [hp_X] in 1 TUBE (0220-5160-41)
Marketing
Marketing Status
Brand
uva ursi
Generic
arctostaphylos uva ursi leaf
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0a35df43-5bf5-c58f-e063-6294a90aa4e0", "openfda": {"unii": ["3M5V3D1X36"], "spl_set_id": ["68591b22-b68f-6c34-e053-2991aa0ab01f"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "8 [hp_X] in 1 TUBE (0220-5160-41)", "package_ndc": "0220-5160-41", "marketing_start_date": "19830303"}], "brand_name": "Uva ursi", "product_id": "0220-5160_0a35df43-5bf5-c58f-e063-6294a90aa4e0", "dosage_form": "PELLET", "product_ndc": "0220-5160", "generic_name": "ARCTOSTAPHYLOS UVA URSI LEAF", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Uva ursi", "active_ingredients": [{"name": "ARCTOSTAPHYLOS UVA-URSI LEAF", "strength": "8 [hp_X]/8[hp_X]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}