Package 43742-1716-1

Brand: boba homo

Generic: babesia microti, borrelia burgdorferi nosode
NDC Package

Package Facts

Identity

Package NDC 43742-1716-1
Digits Only 4374217161
Product NDC 43742-1716
Product ID 43742-1716_f295efbe-3601-4453-b423-bd493d11ade7
Description

30 mL in 1 BOTTLE, DROPPER (43742-1716-1)

Marketing

Marketing Status
Marketed Since 2020-10-07
Brand boba homo
Generic babesia microti, borrelia burgdorferi nosode
Sample Package No

Linked Drug Pages (1)

BOBA HOMO ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f295efbe-3601-4453-b423-bd493d11ade7", "openfda": {"upc": ["0810151882475"], "unii": ["1948X6KEG3", "0J8NV9V5Q8"], "spl_set_id": ["dae13222-a407-4982-8caf-17397a815806"], "manufacturer_name": ["Deseret Biologicals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 mL in 1 BOTTLE, DROPPER (43742-1716-1)", "package_ndc": "43742-1716-1", "marketing_start_date": "20201007"}], "brand_name": "BOBA HOMO", "product_id": "43742-1716_f295efbe-3601-4453-b423-bd493d11ade7", "dosage_form": "LIQUID", "product_ndc": "43742-1716", "generic_name": "Babesia Microti, Borrelia Burgdorferi Nosode", "labeler_name": "Deseret Biologicals, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "BOBA HOMO", "active_ingredients": [{"name": "BABESIA MICROTI", "strength": "15 [hp_X]/mL"}, {"name": "BORRELIA BURGDORFERI", "strength": "15 [hp_X]/mL"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20201007", "listing_expiration_date": "20261231"}