Package 0220-1095-41

Brand: calcarea silicata

Generic: calcium silicate
NDC Package

Package Facts

Identity

Package NDC 0220-1095-41
Digits Only 0220109541
Product NDC 0220-1095
Description

30 [hp_C] in 1 TUBE (0220-1095-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand calcarea silicata
Generic calcium silicate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "09be8cc8-b80d-4600-e063-6294a90a74a2", "openfda": {"unii": ["S4255P4G5M"], "spl_set_id": ["849c4b62-8428-29b7-e053-2a91aa0aede3"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_C] in 1 TUBE (0220-1095-41)", "package_ndc": "0220-1095-41", "marketing_start_date": "19830303"}], "brand_name": "Calcarea silicata", "product_id": "0220-1095_09be8cc8-b80d-4600-e063-6294a90a74a2", "dosage_form": "PELLET", "pharm_class": ["Blood Coagulation Factor [EPC]", "Calcium [CS]", "Cations", "Divalent [CS]", "Increased Coagulation Factor Activity [PE]", "Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "0220-1095", "generic_name": "CALCIUM SILICATE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Calcarea silicata", "active_ingredients": [{"name": "CALCIUM SILICATE", "strength": "30 [hp_C]/30[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}