sevelamer carbonate

Generic: sevelamer carbonate

Labeler: avpak
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sevelamer carbonate
Generic Name sevelamer carbonate
Labeler avpak
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

sevelamer carbonate 800 mg/1

Manufacturer
AvPAK

Identifiers & Regulatory

Product NDC 50268-720
Product ID 50268-720_48d3c3e9-e4a2-5516-e063-6294a90a3dd3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207288
Listing Expiration 2027-12-31
Marketing Start 2019-01-14

Pharmacologic Class

Classes
phosphate binder [epc] phosphate chelating activity [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50268720
Hyphenated Format 50268-720

Supplemental Identifiers

RxCUI
749206
UNII
9YCX42I8IU

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name sevelamer carbonate (source: ndc)
Generic Name sevelamer carbonate (source: ndc)
Application Number ANDA207288 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 800 mg/1
source: ndc
Packaging
  • 50 BLISTER PACK in 1 BOX (50268-720-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-720-11)
source: ndc

Packages (1)

Ingredients (1)

sevelamer carbonate (800 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48d3c3e9-e4a2-5516-e063-6294a90a3dd3", "openfda": {"unii": ["9YCX42I8IU"], "rxcui": ["749206"], "spl_set_id": ["7f701cb4-3089-375f-e053-2991aa0a51b9"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-720-15)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-720-11)", "package_ndc": "50268-720-15", "marketing_start_date": "20190114"}], "brand_name": "Sevelamer Carbonate", "product_id": "50268-720_48d3c3e9-e4a2-5516-e063-6294a90a3dd3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "50268-720", "generic_name": "Sevelamer Carbonate", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sevelamer Carbonate", "active_ingredients": [{"name": "SEVELAMER CARBONATE", "strength": "800 mg/1"}], "application_number": "ANDA207288", "marketing_category": "ANDA", "marketing_start_date": "20190114", "listing_expiration_date": "20271231"}