Package 0220-0999-41

Brand: calcarea sulphurica

Generic: calcium sulfate anhydrous
NDC Package

Package Facts

Identity

Package NDC 0220-0999-41
Digits Only 0220099941
Product NDC 0220-0999
Description

30 [hp_C] in 1 TUBE (0220-0999-41)

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": "f52a1474-11dd-c2b6-e053-2a95a90a44d9", "openfda": {"unii": ["E934B3V59H"], "spl_set_id": ["849cf863-5e33-27ca-e053-2991aa0a04d9"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_C] in 1 TUBE (0220-0999-41)", "package_ndc": "0220-0999-41", "marketing_start_date": "19830303"}], "brand_name": "Calcarea sulphurica", "product_id": "0220-0999_f52a1474-11dd-c2b6-e053-2a95a90a44d9", "dosage_form": "PELLET", "pharm_class": ["Blood Coagulation Factor [EPC]", "Calcium [CS]", "Cations", "Divalent [CS]", "Increased Coagulation Factor Activity [PE]"], "product_ndc": "0220-0999", "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": "30 [hp_C]/30[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}