Package 0220-7838-41

Brand: syphilinum

Generic: treponemic skin canker human
NDC Package

Package Facts

Identity

Package NDC 0220-7838-41
Digits Only 0220783841
Product NDC 0220-7838
Description

30 [hp_C] in 1 TUBE (0220-7838-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand syphilinum
Generic treponemic skin canker human
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0a361e9b-0cdf-f7c7-e063-6294a90a08b7", "openfda": {"unii": ["4ZWP7FWI8W"], "spl_set_id": ["8771de7e-b058-ea00-e053-2a95a90a7512"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_C] in 1 TUBE (0220-7838-41)", "package_ndc": "0220-7838-41", "marketing_start_date": "19830303"}], "brand_name": "Syphilinum", "product_id": "0220-7838_0a361e9b-0cdf-f7c7-e063-6294a90a08b7", "dosage_form": "PELLET", "product_ndc": "0220-7838", "generic_name": "TREPONEMIC SKIN CANKER HUMAN", "labeler_name": "Boiron", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Syphilinum", "active_ingredients": [{"name": "TREPONEMIC SKIN CANKER HUMAN", "strength": "30 [hp_C]/30[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}