Package 0220-4939-41

Brand: tellurium metallicum

Generic: tellurium
NDC Package

Package Facts

Identity

Package NDC 0220-4939-41
Digits Only 0220493941
Product NDC 0220-4939
Description

200 [kp_C] in 1 TUBE (0220-4939-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand tellurium metallicum
Generic tellurium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f528df03-168a-4289-e053-2995a90a4395", "openfda": {"unii": ["NQA0O090ZJ"], "spl_set_id": ["865c6a4e-fc7c-6c98-e053-2991aa0ab685"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-4939-41)", "package_ndc": "0220-4939-41", "marketing_start_date": "19830303"}], "brand_name": "Tellurium metallicum", "product_id": "0220-4939_f528df03-168a-4289-e053-2995a90a4395", "dosage_form": "PELLET", "product_ndc": "0220-4939", "generic_name": "TELLURIUM", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Tellurium metallicum", "active_ingredients": [{"name": "TELLURIUM", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}