Package 0220-0995-41
Brand: calcarea sulphurica
Generic: calcium sulfate anhydrousPackage Facts
Identity
Package NDC
0220-0995-41
Digits Only
0220099541
Product NDC
0220-0995
Description
12 [hp_C] in 1 TUBE (0220-0995-41)
Marketing
Marketing Status
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": "09badbb9-8fae-120a-e063-6294a90ad032", "openfda": {"unii": ["E934B3V59H"], "spl_set_id": ["849cb2cd-cc36-05f1-e053-2991aa0ab2f7"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 [hp_C] in 1 TUBE (0220-0995-41)", "package_ndc": "0220-0995-41", "marketing_start_date": "19830303"}], "brand_name": "Calcarea sulphurica", "product_id": "0220-0995_09badbb9-8fae-120a-e063-6294a90ad032", "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": "0220-0995", "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": "12 [hp_C]/12[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}