Package 0220-0848-41
Brand: beryllium metallicum
Generic: berylliumPackage Facts
Identity
Package NDC
0220-0848-41
Digits Only
0220084841
Product NDC
0220-0848
Description
200 [kp_C] in 1 TUBE (0220-0848-41)
Marketing
Marketing Status
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": "09bac992-8027-5dee-e063-6394a90a7e0d", "openfda": {"unii": ["OW5102UV6N"], "spl_set_id": ["850136ef-8fcf-7c09-e053-2a91aa0a6abd"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-0848-41)", "package_ndc": "0220-0848-41", "marketing_start_date": "19830303"}], "brand_name": "Beryllium metallicum", "product_id": "0220-0848_09bac992-8027-5dee-e063-6394a90a7e0d", "dosage_form": "PELLET", "product_ndc": "0220-0848", "generic_name": "BERYLLIUM", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Beryllium metallicum", "active_ingredients": [{"name": "BERYLLIUM", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}