Package 60687-449-01

Brand: sevelamer hydrochloride

Generic: sevelamer hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60687-449-01
Digits Only 6068744901
Product NDC 60687-449
Description

100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-449-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-449-11)

Marketing

Marketing Status
Marketed Since 2020-01-22
Brand sevelamer hydrochloride
Generic sevelamer hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "26408f23-0427-1bed-e063-6394a90aa7c8", "openfda": {"unii": ["GLS2PGI8QG"], "rxcui": ["857224"], "spl_set_id": ["8830526f-d957-423e-84ea-e4d79346948b"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-449-01)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-449-11)", "package_ndc": "60687-449-01", "marketing_start_date": "20200122"}], "brand_name": "Sevelamer Hydrochloride", "product_id": "60687-449_26408f23-0427-1bed-e063-6394a90aa7c8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "60687-449", "generic_name": "Sevelamer Hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sevelamer Hydrochloride", "active_ingredients": [{"name": "SEVELAMER HYDROCHLORIDE", "strength": "800 mg/1"}], "application_number": "ANDA204724", "marketing_category": "ANDA", "marketing_start_date": "20200122", "listing_expiration_date": "20261231"}