Package 0220-4990-41

Brand: thiosinominum

Generic: allylthiourea
NDC Package

Package Facts

Identity

Package NDC 0220-4990-41
Digits Only 0220499041
Product NDC 0220-4990
Product ID 0220-4990_0a349bfa-bb8a-ddb1-e063-6294a90a5772
Description

6 [hp_X] in 1 TUBE (0220-4990-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand thiosinominum
Generic allylthiourea
Sample Package No

Linked Drug Pages (1)

Thiosinominum ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0a349bfa-bb8a-ddb1-e063-6294a90a5772", "openfda": {"unii": ["706IDJ14B7"], "spl_set_id": ["8773567e-26ba-0ed6-e053-2995a90aff91"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 [hp_X] in 1 TUBE (0220-4990-41)", "package_ndc": "0220-4990-41", "marketing_start_date": "19830303"}], "brand_name": "Thiosinominum", "product_id": "0220-4990_0a349bfa-bb8a-ddb1-e063-6294a90a5772", "dosage_form": "PELLET", "product_ndc": "0220-4990", "generic_name": "ALLYLTHIOUREA", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Thiosinominum", "active_ingredients": [{"name": "ALLYLTHIOUREA", "strength": "6 [hp_X]/6[hp_X]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}