calcium acetate
Generic: calcium acetate
Labeler: avkareDrug Facts
Product Profile
Brand Name
calcium acetate
Generic Name
calcium acetate
Labeler
avkare
Dosage Form
CAPSULE
Routes
Active Ingredients
calcium acetate 667 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
73190-031
Product ID
73190-031_35a6eb8e-624d-2222-e063-6394a90ab589
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA202315
Listing Expiration
2026-12-31
Marketing Start
2025-05-21
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
73190031
Hyphenated Format
73190-031
Supplemental Identifiers
RxCUI
UPC
UNII
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
ANDA202315 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 667 mg/1
Packaging
- 200 CAPSULE in 1 BOTTLE (73190-031-20)
Packages (1)
Ingredients (1)
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"}