Package 0220-1775-41
Brand: dioscorea villosa
Generic: dioscorea villosa tuberPackage Facts
Identity
Package NDC
0220-1775-41
Digits Only
0220177541
Product NDC
0220-1775
Description
9 [hp_C] in 1 TUBE (0220-1775-41)
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": "0a0c9e7f-6ddc-b628-e063-6394a90a5916", "openfda": {"unii": ["IWY3IWX2G8"], "spl_set_id": ["7a2e39f5-f656-14c7-e053-2a91aa0a3fa1"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "9 [hp_C] in 1 TUBE (0220-1775-41)", "package_ndc": "0220-1775-41", "marketing_start_date": "19830303"}], "brand_name": "Dioscorea villosa", "product_id": "0220-1775_0a0c9e7f-6ddc-b628-e063-6394a90a5916", "dosage_form": "PELLET", "product_ndc": "0220-1775", "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": "9 [hp_C]/9[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}