calcium acetate
Generic: calcium acetate
Labeler: square pharmaceuticals limitedDrug Facts
Product Profile
Brand Name
calcium acetate
Generic Name
calcium acetate
Labeler
square pharmaceuticals limited
Dosage Form
CAPSULE
Routes
Active Ingredients
calcium acetate 667 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
76483-086
Product ID
76483-086_6561c80c-48b4-4318-a28c-7cca27cd2885
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA217205
Listing Expiration
2026-12-31
Marketing Start
2023-05-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
76483086
Hyphenated Format
76483-086
Supplemental Identifiers
RxCUI
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
ANDA217205 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 667 mg/1
Packaging
- 200 CAPSULE in 1 BOTTLE (76483-086-00)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6561c80c-48b4-4318-a28c-7cca27cd2885", "openfda": {"unii": ["Y882YXF34X"], "rxcui": ["359296"], "spl_set_id": ["5af79d16-31ad-4d68-9a6d-bb5d9c91535d"], "manufacturer_name": ["SQUARE PHARMACEUTICALS LIMITED"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 CAPSULE in 1 BOTTLE (76483-086-00)", "package_ndc": "76483-086-00", "marketing_start_date": "20230531"}], "brand_name": "Calcium Acetate", "product_id": "76483-086_6561c80c-48b4-4318-a28c-7cca27cd2885", "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": "76483-086", "generic_name": "Calcium Acetate", "labeler_name": "SQUARE PHARMACEUTICALS LIMITED", "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": "20230531", "listing_expiration_date": "20261231"}