Package 62135-192-22

Brand: calcium acetate

Generic: calcium acetate
NDC Package

Package Facts

Identity

Package NDC 62135-192-22
Digits Only 6213519222
Product NDC 62135-192
Description

200 TABLET in 1 BOTTLE (62135-192-22)

Marketing

Marketing Status
Marketed Since 2019-07-01
Brand calcium acetate
Generic calcium acetate
Sample Package No

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"}