Package 0220-3055-41

Brand: lapis albus

Generic: calcium hexafluorosilicate
NDC Package

Package Facts

Identity

Package NDC 0220-3055-41
Digits Only 0220305541
Product NDC 0220-3055
Product ID 0220-3055_0a0e30cc-ad7f-8cf3-e063-6394a90a974d
Description

9 [hp_C] in 1 TUBE (0220-3055-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand lapis albus
Generic calcium hexafluorosilicate
Sample Package No

Linked Drug Pages (1)

Lapis albus ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0a0e30cc-ad7f-8cf3-e063-6394a90a974d", "openfda": {"unii": ["2NVP93XVQ3"], "spl_set_id": ["861bb302-0d92-0aa2-e053-2a91aa0a52cf"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "9 [hp_C] in 1 TUBE (0220-3055-41)", "package_ndc": "0220-3055-41", "marketing_start_date": "19830303"}], "brand_name": "Lapis albus", "product_id": "0220-3055_0a0e30cc-ad7f-8cf3-e063-6394a90a974d", "dosage_form": "PELLET", "product_ndc": "0220-3055", "generic_name": "CALCIUM HEXAFLUOROSILICATE", "labeler_name": "Boiron", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lapis albus", "active_ingredients": [{"name": "CALCIUM HEXAFLUOROSILICATE", "strength": "9 [hp_C]/9[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}