Package 0904-7209-06
Brand: sevelamer hydrochloride
Generic: sevelamer hydrochloridePackage Facts
Identity
Package NDC
0904-7209-06
Digits Only
0904720906
Product NDC
0904-7209
Description
50 BLISTER PACK in 1 CARTON (0904-7209-06) / 1 TABLET, FILM COATED in 1 BLISTER PACK
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": ["PARENTERAL"], "spl_id": "53f9bd53-115d-48b3-b273-55e75d6a16a5", "openfda": {"unii": ["GLS2PGI8QG"], "rxcui": ["857224"], "spl_set_id": ["0500034d-458c-42c5-918d-9acd22f0c28b"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 CARTON (0904-7209-06) / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-7209-06", "marketing_start_date": "20240819"}], "brand_name": "sevelamer hydrochloride", "product_id": "0904-7209_53f9bd53-115d-48b3-b273-55e75d6a16a5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "0904-7209", "generic_name": "sevelamer hydrochloride", "labeler_name": "Major Pharmaceuticals", "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": "20240819", "listing_expiration_date": "20271231"}