Package 0220-0839-41

Brand: beryllium metallicum

Generic: beryllium
NDC Package

Package Facts

Identity

Package NDC 0220-0839-41
Digits Only 0220083941
Product NDC 0220-0839
Description

30 [hp_C] in 1 TUBE (0220-0839-41)

Marketing

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

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "09bab81a-261b-df3a-e063-6294a90a67dd", "openfda": {"unii": ["OW5102UV6N"], "spl_set_id": ["687fca4c-11bb-fda9-e053-2a91aa0a146b"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_C] in 1 TUBE (0220-0839-41)", "package_ndc": "0220-0839-41", "marketing_start_date": "19830303"}], "brand_name": "Beryllium metallicum", "product_id": "0220-0839_09bab81a-261b-df3a-e063-6294a90a67dd", "dosage_form": "PELLET", "product_ndc": "0220-0839", "generic_name": "BERYLLIUM", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Beryllium metallicum", "active_ingredients": [{"name": "BERYLLIUM", "strength": "30 [hp_C]/30[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}