Package 0220-1773-41
Brand: dioscorea villosa
Generic: dioscorea villosa tuberPackage Facts
Identity
Package NDC
0220-1773-41
Digits Only
0220177341
Product NDC
0220-1773
Description
30 [hp_C] in 1 TUBE (0220-1773-41)
Marketing
Marketing Status
Brand
dioscorea villosa
Generic
dioscorea villosa tuber
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0a0c7444-3a86-a6ce-e063-6394a90a0422", "openfda": {"unii": ["IWY3IWX2G8"], "spl_set_id": ["857b811c-7b16-206a-e053-2991aa0a16fa"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_C] in 1 TUBE (0220-1773-41)", "package_ndc": "0220-1773-41", "marketing_start_date": "19830303"}], "brand_name": "Dioscorea villosa", "product_id": "0220-1773_0a0c7444-3a86-a6ce-e063-6394a90a0422", "dosage_form": "PELLET", "product_ndc": "0220-1773", "generic_name": "DIOSCOREA VILLOSA TUBER", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Dioscorea villosa", "active_ingredients": [{"name": "DIOSCOREA VILLOSA TUBER", "strength": "30 [hp_C]/30[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}