calcium acetate

Generic: calcium acetate

Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name calcium acetate
Generic Name calcium acetate
Labeler heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

calcium acetate 667 mg/1

Manufacturer
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 23155-621
Product ID 23155-621_43972e52-b7af-4a00-b77c-1f37ad9cd811
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202885
Listing Expiration 2026-12-31
Marketing Start 2015-01-22

Pharmacologic Class

Classes
blood coagulation factor [epc] calcium [cs] cations divalent [cs] increased coagulation factor activity [pe] phosphate binder [epc] phosphate chelating activity [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 23155621
Hyphenated Format 23155-621

Supplemental Identifiers

RxCUI
197433
UPC
0323155621020
UNII
Y882YXF34X

Packaging Origin

Original Packager
true

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 ANDA202885 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 667 mg/1
source: ndc
Packaging
  • 200 TABLET in 1 BOTTLE (23155-621-02)
source: ndc

Packages (1)

23155-621-02 200 TABLET in 1 BOTTLE (23155-621-02)

Ingredients (1)

calcium acetate (667 mg/1)

Linked Drug Pages (1)

CALCIUM ACETATE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "43972e52-b7af-4a00-b77c-1f37ad9cd811", "openfda": {"upc": ["0323155621020"], "unii": ["Y882YXF34X"], "rxcui": ["197433"], "spl_set_id": ["ac4975aa-0ee9-4473-81e2-839f1556e684"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 TABLET in 1 BOTTLE (23155-621-02)", "package_ndc": "23155-621-02", "marketing_start_date": "20150122"}], "brand_name": "CALCIUM ACETATE", "product_id": "23155-621_43972e52-b7af-4a00-b77c-1f37ad9cd811", "dosage_form": "TABLET", "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": "23155-621", "generic_name": "CALCIUM ACETATE", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CALCIUM ACETATE", "active_ingredients": [{"name": "CALCIUM ACETATE", "strength": "667 mg/1"}], "application_number": "ANDA202885", "marketing_category": "ANDA", "marketing_start_date": "20150122", "listing_expiration_date": "20261231"}