sevelamer carbonate

Generic: sevelamer carbonate

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

sevelamer carbonate 800 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-328
Product ID 60687-328_1e7c0036-b057-e32a-e063-6394a90a6caf
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207179
Listing Expiration 2026-12-31
Marketing Start 2017-08-22

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687328
Hyphenated Format 60687-328

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 ANDA207179 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 800 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-328-31) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-328-33)
  • 50 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-328-65) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-328-11)
source: ndc

Packages (2)

60687-328-31 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-328-31) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-328-33) 60687-328-65 50 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-328-65) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-328-11)

Ingredients (1)

sevelamer carbonate (800 mg/1)

Linked Drug Pages (1)

Sevelamer Carbonate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1e7c0036-b057-e32a-e063-6394a90a6caf", "openfda": {"unii": ["9YCX42I8IU"], "rxcui": ["749206"], "spl_set_id": ["bd0a89ab-91c4-42b3-aa88-1e3295d0d344"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-328-31)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-328-33)", "package_ndc": "60687-328-31", "marketing_start_date": "20170822"}, {"sample": false, "description": "50 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-328-65)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-328-11)", "package_ndc": "60687-328-65", "marketing_start_date": "20190424"}], "brand_name": "Sevelamer Carbonate", "product_id": "60687-328_1e7c0036-b057-e32a-e063-6394a90a6caf", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "60687-328", "generic_name": "Sevelamer Carbonate", "labeler_name": "American Health Packaging", "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": "20170822", "listing_expiration_date": "20261231"}