Package 76282-664-27

Brand: sevelamer carbonate

Generic: sevelamer carbonate
NDC Package

Package Facts

Identity

Package NDC 76282-664-27
Digits Only 7628266427
Product NDC 76282-664
Product ID 76282-664_831095de-d22d-496d-834c-c4505e639c87
Description

270 TABLET, FILM COATED in 1 BOTTLE (76282-664-27)

Marketing

Marketing Status
Marketed Since 2019-08-08
Brand sevelamer carbonate
Generic sevelamer carbonate
Sample Package No

Linked Drug Pages (1)

Sevelamer carbonate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "831095de-d22d-496d-834c-c4505e639c87", "openfda": {"unii": ["9YCX42I8IU"], "rxcui": ["749206"], "spl_set_id": ["f8947f65-57be-4af7-b0e7-17666f496d01"], "manufacturer_name": ["Exelan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "270 TABLET, FILM COATED in 1 BOTTLE (76282-664-27)", "package_ndc": "76282-664-27", "marketing_start_date": "20190808"}], "brand_name": "Sevelamer carbonate", "product_id": "76282-664_831095de-d22d-496d-834c-c4505e639c87", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "76282-664", "generic_name": "SEVELAMER CARBONATE", "labeler_name": "Exelan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sevelamer carbonate", "active_ingredients": [{"name": "SEVELAMER CARBONATE", "strength": "800 mg/1"}], "application_number": "ANDA203860", "marketing_category": "ANDA", "marketing_start_date": "20171026", "listing_expiration_date": "20261231"}