Package 73190-031-20
Brand: calcium acetate
Generic: calcium acetatePackage Facts
Identity
Package NDC
73190-031-20
Digits Only
7319003120
Product NDC
73190-031
Description
200 CAPSULE in 1 BOTTLE (73190-031-20)
Marketing
Marketing Status
Brand
calcium acetate
Generic
calcium acetate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "35a6eb8e-624d-2222-e063-6394a90ab589", "openfda": {"upc": ["0373190031209"], "unii": ["Y882YXF34X"], "rxcui": ["359296"], "spl_set_id": ["35a6f515-dfe7-031c-e063-6294a90a5e95"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "200 CAPSULE in 1 BOTTLE (73190-031-20)", "package_ndc": "73190-031-20", "marketing_start_date": "20250521"}], "brand_name": "calcium acetate", "product_id": "73190-031_35a6eb8e-624d-2222-e063-6394a90ab589", "dosage_form": "CAPSULE", "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": "73190-031", "generic_name": "calcium acetate", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "calcium acetate", "active_ingredients": [{"name": "CALCIUM ACETATE", "strength": "667 mg/1"}], "application_number": "ANDA202315", "marketing_category": "ANDA", "marketing_start_date": "20250521", "listing_expiration_date": "20261231"}