Package 16714-814-01

Brand: sevelamer carbonate

Generic: sevelamer carbonate
NDC Package

Package Facts

Identity

Package NDC 16714-814-01
Digits Only 1671481401
Product NDC 16714-814
Product ID 16714-814_a2199a9d-47ad-4994-ba6f-af6e4d1ad7da
Description

270 TABLET, FILM COATED in 1 BOTTLE (16714-814-01)

Marketing

Marketing Status
Marketed Since 2018-06-06
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": "a2199a9d-47ad-4994-ba6f-af6e4d1ad7da", "openfda": {"unii": ["9YCX42I8IU"], "rxcui": ["749206"], "spl_set_id": ["9b4d0720-f4e7-4b4f-affc-57ce8bb0b722"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "270 TABLET, FILM COATED in 1 BOTTLE (16714-814-01)", "package_ndc": "16714-814-01", "marketing_start_date": "20180606"}], "brand_name": "Sevelamer Carbonate", "product_id": "16714-814_a2199a9d-47ad-4994-ba6f-af6e4d1ad7da", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "16714-814", "generic_name": "Sevelamer Carbonate", "labeler_name": "NorthStar Rx LLC", "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": "20180606", "listing_expiration_date": "20261231"}