Package 0220-0378-41
Brand: antimonium tartaricum
Generic: antimony potassium tartratePackage Facts
Identity
Package NDC
0220-0378-41
Digits Only
0220037841
Product NDC
0220-0378
Description
9 [hp_C] in 1 TUBE (0220-0378-41)
Marketing
Marketing Status
Brand
antimonium tartaricum
Generic
antimony potassium tartrate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f1874165-9c3c-0aec-e053-2a95a90ac93d", "openfda": {"unii": ["DL6OZ476V3"], "spl_set_id": ["845f7da9-a4de-27e0-e053-2991aa0a0f40"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "9 [hp_C] in 1 TUBE (0220-0378-41)", "package_ndc": "0220-0378-41", "marketing_start_date": "19830303"}], "brand_name": "Antimonium tartaricum", "product_id": "0220-0378_f1874165-9c3c-0aec-e053-2a95a90ac93d", "dosage_form": "PELLET", "product_ndc": "0220-0378", "generic_name": "ANTIMONY POTASSIUM TARTRATE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Antimonium tartaricum", "active_ingredients": [{"name": "ANTIMONY POTASSIUM TARTRATE", "strength": "9 [hp_C]/9[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}