Package 66096-785-01
Brand: antimonium tartaricum
Generic: antimonium tartaricumPackage Facts
Identity
Package NDC
66096-785-01
Digits Only
6609678501
Product NDC
66096-785
Description
6 [hp_C] in 1 TUBE (66096-785-01)
Marketing
Marketing Status
Brand
antimonium tartaricum
Generic
antimonium tartaricum
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d450927c-8450-efd6-e053-2a95a90a4f4e", "openfda": {"unii": ["DL6OZ476V3"], "spl_set_id": ["775cd22f-54fc-43f5-becc-724eb26f2fc0"], "manufacturer_name": ["OHM PHARMA INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 [hp_C] in 1 TUBE (66096-785-01)", "package_ndc": "66096-785-01", "marketing_start_date": "20191101"}], "brand_name": "Antimonium Tartaricum", "product_id": "66096-785_d450927c-8450-efd6-e053-2a95a90a4f4e", "dosage_form": "PELLET", "product_ndc": "66096-785", "generic_name": "ANTIMONIUM TARTARICUM", "labeler_name": "OHM PHARMA INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Antimonium Tartaricum", "active_ingredients": [{"name": "ANTIMONY POTASSIUM TARTRATE", "strength": "6 [hp_C]/6[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20191101", "listing_expiration_date": "20261231"}