Package 72789-422-97

Brand: calcium acetate

Generic: calcium acetate
NDC Package

Package Facts

Identity

Package NDC 72789-422-97
Digits Only 7278942297
Product NDC 72789-422
Description

200 CAPSULE in 1 BOTTLE, PLASTIC (72789-422-97)

Marketing

Marketing Status
Marketed Since 2024-07-16
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": "4123b0e5-2fcd-88fb-e063-6294a90a05e7", "openfda": {"upc": ["0372789422978"], "unii": ["Y882YXF34X"], "rxcui": ["359296"], "spl_set_id": ["925918d5-9f89-4f2f-9bb9-d9c53d90bb0a"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "200 CAPSULE in 1 BOTTLE, PLASTIC (72789-422-97)", "package_ndc": "72789-422-97", "marketing_start_date": "20240716"}], "brand_name": "Calcium Acetate", "product_id": "72789-422_4123b0e5-2fcd-88fb-e063-6294a90a05e7", "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": "72789-422", "generic_name": "Calcium Acetate", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Calcium Acetate", "active_ingredients": [{"name": "CALCIUM ACETATE", "strength": "667 mg/1"}], "application_number": "ANDA217205", "marketing_category": "ANDA", "marketing_start_date": "20231207", "listing_expiration_date": "20261231"}