Package 0220-1000-41

Brand: calcarea sulphurica

Generic: calcium sulfate anhydrous
NDC Package

Package Facts

Identity

Package NDC 0220-1000-41
Digits Only 0220100041
Product NDC 0220-1000
Description

200 [kp_C] in 1 TUBE (0220-1000-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand calcarea sulphurica
Generic calcium sulfate anhydrous
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "09bacb67-af65-06fe-e063-6294a90acf35", "openfda": {"unii": ["E934B3V59H"], "spl_set_id": ["8513ef0f-9cf7-736d-e053-2991aa0a416c"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-1000-41)", "package_ndc": "0220-1000-41", "marketing_start_date": "19830303"}], "brand_name": "Calcarea sulphurica", "product_id": "0220-1000_09bacb67-af65-06fe-e063-6294a90acf35", "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": "0220-1000", "generic_name": "CALCIUM SULFATE ANHYDROUS", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Calcarea sulphurica", "active_ingredients": [{"name": "CALCIUM SULFATE ANHYDROUS", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}