calcium acetate
Generic: calcium acetate
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
calcium acetate
Generic Name
calcium acetate
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
calcium acetate 667 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72789-422
Product ID
72789-422_4123b0e5-2fcd-88fb-e063-6294a90a05e7
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA217205
Listing Expiration
2026-12-31
Marketing Start
2023-12-07
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72789422
Hyphenated Format
72789-422
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
ANDA217205 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 667 mg/1
Packaging
- 200 CAPSULE in 1 BOTTLE, PLASTIC (72789-422-97)
Packages (1)
Ingredients (1)
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"}