Package 69367-411-02

Brand: calcium acetate

Generic: calcium acetate
NDC Package

Package Facts

Identity

Package NDC 69367-411-02
Digits Only 6936741102
Product NDC 69367-411
Description

200 CAPSULE in 1 BOTTLE (69367-411-02)

Marketing

Marketing Status
Marketed Since 2025-06-13
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": "1cfbc903-9b50-4baf-bded-600c80240a0f", "openfda": {"upc": ["0369367411028"], "unii": ["Y882YXF34X"], "rxcui": ["359296"], "spl_set_id": ["1195f5d5-db91-4b9e-86ad-be340b43d690"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 CAPSULE in 1 BOTTLE (69367-411-02)", "package_ndc": "69367-411-02", "marketing_start_date": "20250613"}], "brand_name": "Calcium Acetate", "product_id": "69367-411_1cfbc903-9b50-4baf-bded-600c80240a0f", "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": "69367-411", "generic_name": "Calcium Acetate", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Calcium Acetate", "active_ingredients": [{"name": "CALCIUM ACETATE", "strength": "667 mg/1"}], "application_number": "ANDA203179", "marketing_category": "ANDA", "marketing_start_date": "20250613", "listing_expiration_date": "20271231"}