Package 71205-966-67
Brand: sevelamer carbonate
Generic: sevelamer carbonatePackage Facts
Identity
Package NDC
71205-966-67
Digits Only
7120596667
Product NDC
71205-966
Description
270 TABLET, FILM COATED in 1 BOTTLE (71205-966-67)
Marketing
Marketing Status
Brand
sevelamer carbonate
Generic
sevelamer carbonate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "09aa537e-9f9c-4c0e-9ebf-59a4cf105ee4", "openfda": {"upc": ["0371205966676"], "unii": ["9YCX42I8IU"], "rxcui": ["749206"], "spl_set_id": ["ee9da697-2d55-48e5-8e03-c64c8aaf1fb8"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "270 TABLET, FILM COATED in 1 BOTTLE (71205-966-67)", "package_ndc": "71205-966-67", "marketing_end_date": "20271130", "marketing_start_date": "20200609"}], "brand_name": "Sevelamer Carbonate", "product_id": "71205-966_09aa537e-9f9c-4c0e-9ebf-59a4cf105ee4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "71205-966", "generic_name": "Sevelamer Carbonate", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sevelamer Carbonate", "active_ingredients": [{"name": "SEVELAMER CARBONATE", "strength": "800 mg/1"}], "application_number": "ANDA200959", "marketing_category": "ANDA", "marketing_end_date": "20271130", "marketing_start_date": "20190930"}