Package 60687-449-01
Brand: sevelamer hydrochloride
Generic: sevelamer hydrochloridePackage 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
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"}