calcium acetate
Generic: calcium acetate
Labeler: chartwell rx llcDrug Facts
Product Profile
Brand Name
calcium acetate
Generic Name
calcium acetate
Labeler
chartwell rx llc
Dosage Form
TABLET
Routes
Active Ingredients
calcium acetate 667 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
62135-192
Product ID
62135-192_2471197e-c8a7-c3c7-e063-6394a90a16d7
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA202420
Listing Expiration
2026-12-31
Marketing Start
2019-07-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
62135192
Hyphenated Format
62135-192
Supplemental Identifiers
RxCUI
UPC
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
ANDA202420 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 667 mg/1
Packaging
- 200 TABLET in 1 BOTTLE (62135-192-22)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2471197e-c8a7-c3c7-e063-6394a90a16d7", "openfda": {"upc": ["0362135192228"], "unii": ["Y882YXF34X"], "rxcui": ["197433"], "spl_set_id": ["9584350a-b6ad-45ae-b1c5-c8ca8f471c03"], "manufacturer_name": ["Chartwell RX LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 TABLET in 1 BOTTLE (62135-192-22)", "package_ndc": "62135-192-22", "marketing_start_date": "20190701"}], "brand_name": "Calcium Acetate", "product_id": "62135-192_2471197e-c8a7-c3c7-e063-6394a90a16d7", "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": "62135-192", "generic_name": "Calcium Acetate", "labeler_name": "Chartwell RX LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Calcium Acetate", "active_ingredients": [{"name": "CALCIUM ACETATE", "strength": "667 mg/1"}], "application_number": "ANDA202420", "marketing_category": "ANDA", "marketing_start_date": "20190701", "listing_expiration_date": "20261231"}