Package 17856-0921-1

Brand: sevelamer carbonate

Generic: sevelamer carbonate
NDC Package

Package Facts

Identity

Package NDC 17856-0921-1
Digits Only 1785609211
Product NDC 17856-0921
Description

100 POUCH in 1 CASE (17856-0921-1) / 1 TABLET, FILM COATED in 1 POUCH (17856-0921-2)

Marketing

Marketing Status
Marketed Since 2024-05-09
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": "38930d7d-8bbb-c1f4-e063-6394a90a636e", "openfda": {"unii": ["9YCX42I8IU"], "rxcui": ["749206"], "spl_set_id": ["07b709fd-a2a1-4ff1-ad19-827d38e84562"], "manufacturer_name": ["ATLANTIC BIOLOGICALS CORP."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 CASE (17856-0921-1)  / 1 TABLET, FILM COATED in 1 POUCH (17856-0921-2)", "package_ndc": "17856-0921-1", "marketing_start_date": "20240509"}], "brand_name": "Sevelamer Carbonate", "product_id": "17856-0921_38930d7d-8bbb-c1f4-e063-6394a90a636e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "17856-0921", "generic_name": "Sevelamer Carbonate", "labeler_name": "ATLANTIC BIOLOGICALS CORP.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sevelamer Carbonate", "active_ingredients": [{"name": "SEVELAMER CARBONATE", "strength": "800 mg/1"}], "application_number": "ANDA207179", "marketing_category": "ANDA", "marketing_start_date": "20180627", "listing_expiration_date": "20261231"}