calcium acetate
Generic: calcium acetate
Labeler: westminster pharmaceuticals, llcDrug Facts
Product Profile
Brand Name
calcium acetate
Generic Name
calcium acetate
Labeler
westminster pharmaceuticals, llc
Dosage Form
CAPSULE
Routes
Active Ingredients
calcium acetate 667 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
69367-411
Product ID
69367-411_1cfbc903-9b50-4baf-bded-600c80240a0f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA203179
Listing Expiration
2027-12-31
Marketing Start
2025-06-13
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69367411
Hyphenated Format
69367-411
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
calcium acetate (source: ndc)
Generic Name
calcium acetate (source: ndc)
Application Number
ANDA203179 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 667 mg/1
Packaging
- 200 CAPSULE in 1 BOTTLE (69367-411-02)
Packages (1)
Ingredients (1)
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"}