calcium acetate
Generic: calcium acetate
Labeler: major pharmaceuticalsDrug Facts
Product Profile
Brand Name
calcium acetate
Generic Name
calcium acetate
Labeler
major pharmaceuticals
Dosage Form
CAPSULE
Routes
Active Ingredients
calcium acetate 667 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0904-7119
Product ID
0904-7119_d1fb6310-64fc-4bd9-b6bd-9d87ee4f3bc2
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077728
Listing Expiration
2026-12-31
Marketing Start
2008-02-26
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
09047119
Hyphenated Format
0904-7119
Supplemental Identifiers
RxCUI
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
ANDA077728 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 667 mg/1
Packaging
- 50 BLISTER PACK in 1 CARTON (0904-7119-06) / 1 CAPSULE in 1 BLISTER PACK
- 100 BLISTER PACK in 1 CARTON (0904-7119-61) / 1 CAPSULE in 1 BLISTER PACK
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d1fb6310-64fc-4bd9-b6bd-9d87ee4f3bc2", "openfda": {"unii": ["Y882YXF34X"], "rxcui": ["359296"], "spl_set_id": ["9a731cdf-6488-44ca-b97f-512a0e9deab1"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 CARTON (0904-7119-06) / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "0904-7119-06", "marketing_start_date": "20080226"}, {"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7119-61) / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "0904-7119-61", "marketing_start_date": "20080226"}], "brand_name": "Calcium Acetate", "product_id": "0904-7119_d1fb6310-64fc-4bd9-b6bd-9d87ee4f3bc2", "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": "0904-7119", "generic_name": "Calcium Acetate", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Calcium Acetate", "active_ingredients": [{"name": "CALCIUM ACETATE", "strength": "667 mg/1"}], "application_number": "ANDA077728", "marketing_category": "ANDA", "marketing_start_date": "20080226", "listing_expiration_date": "20261231"}