Package 0220-0375-41

Brand: antimonium tartaricum

Generic: antimony potassium tartrate
NDC Package

Package Facts

Identity

Package NDC 0220-0375-41
Digits Only 0220037541
Product NDC 0220-0375
Description

30 [hp_X] in 1 TUBE (0220-0375-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
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": "f911080f-2c49-2a92-e053-6294a90a6923", "openfda": {"unii": ["DL6OZ476V3"], "spl_set_id": ["84ec433c-7d1d-958b-e053-2991aa0a5b71"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_X] in 1 TUBE (0220-0375-41)", "package_ndc": "0220-0375-41", "marketing_start_date": "19830303"}], "brand_name": "Antimonium tartaricum", "product_id": "0220-0375_f911080f-2c49-2a92-e053-6294a90a6923", "dosage_form": "PELLET", "product_ndc": "0220-0375", "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": "30 [hp_X]/30[hp_X]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}