Package 16571-813-20

Brand: calcium acetate

Generic: calcium acetate
NDC Package

Package Facts

Identity

Package NDC 16571-813-20
Digits Only 1657181320
Product NDC 16571-813
Description

200 CAPSULE in 1 BOTTLE, PLASTIC (16571-813-20)

Marketing

Marketing Status
Marketed Since 2021-11-01
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": "f2fd0134-44cd-4d74-835f-980de3e5d9c0", "openfda": {"unii": ["Y882YXF34X"], "rxcui": ["359296"], "spl_set_id": ["ce650ba5-fb42-e444-e053-2a95a90a075a"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 CAPSULE in 1 BOTTLE, PLASTIC (16571-813-20)", "package_ndc": "16571-813-20", "marketing_start_date": "20211101"}], "brand_name": "Calcium Acetate", "product_id": "16571-813_f2fd0134-44cd-4d74-835f-980de3e5d9c0", "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": "16571-813", "generic_name": "Calcium Acetate", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Calcium Acetate", "active_ingredients": [{"name": "CALCIUM ACETATE", "strength": "667 mg/1"}], "application_number": "ANDA211038", "marketing_category": "ANDA", "marketing_start_date": "20211101", "listing_expiration_date": "20261231"}