Package 0220-3968-41

Brand: pertussinum

Generic: human sputum, bordetella pertussis infected
NDC Package

Package Facts

Identity

Package NDC 0220-3968-41
Digits Only 0220396841
Product NDC 0220-3968
Product ID 0220-3968_0a213597-7c17-54ba-e063-6394a90a301b
Description

30 [hp_C] in 1 TUBE (0220-3968-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand pertussinum
Generic human sputum, bordetella pertussis infected
Sample Package No

Linked Drug Pages (1)

Pertussinum ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0a213597-7c17-54ba-e063-6394a90a301b", "openfda": {"unii": ["U364V64HUN"], "spl_set_id": ["875c1597-da1f-46df-e053-2995a90a0bd0"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_C] in 1 TUBE (0220-3968-41)", "package_ndc": "0220-3968-41", "marketing_start_date": "19830303"}], "brand_name": "Pertussinum", "product_id": "0220-3968_0a213597-7c17-54ba-e063-6394a90a301b", "dosage_form": "PELLET", "product_ndc": "0220-3968", "generic_name": "HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED", "labeler_name": "Boiron", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pertussinum", "active_ingredients": [{"name": "HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED", "strength": "30 [hp_C]/30[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}