Drugs@FDA: FDA Approved Drug Products

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Abbreviated New Drug Application (ANDA): 205727
Company: BELCHER PHARMS LLC
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
SODIUM POLYSTYRENE SULFONATE SODIUM POLYSTYRENE SULFONATE 454GM/BOT POWDER;ORAL, RECTAL Prescription AA No No
Original Approvals or Tentative Approvals
Action Date Submission Action Type Submission Classification Review Priority; Orphan Status Letters, Reviews, Labels, Patient Package Insert Notes Url
02/23/2016 ORIG-1 Approval STANDARD

Label is not available on this site.

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
03/16/2018 SUPPL-1 Labeling-Package Insert

Label is not available on this site.

SODIUM POLYSTYRENE SULFONATE

POWDER;ORAL, RECTAL; 454GM/BOT
TE Code = AA

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
KALEXATE SODIUM POLYSTYRENE SULFONATE 454GM/BOT POWDER;ORAL, RECTAL Prescription No AA 040905 KVK TECH
KIONEX SODIUM POLYSTYRENE SULFONATE 454GM/BOT POWDER;ORAL, RECTAL Prescription No AA 040029 PADDOCK LLC
SODIUM POLYSTYRENE SULFONATE SODIUM POLYSTYRENE SULFONATE 454GM/BOT POWDER;ORAL, RECTAL Prescription No AA 206815 APNAR PHARMA LP
SODIUM POLYSTYRENE SULFONATE SODIUM POLYSTYRENE SULFONATE 454GM/BOT POWDER;ORAL, RECTAL Prescription No AA 205727 BELCHER PHARMS LLC
SODIUM POLYSTYRENE SULFONATE SODIUM POLYSTYRENE SULFONATE 454GM/BOT POWDER;ORAL, RECTAL Prescription No AA 089910 CMP PHARMA INC
SODIUM POLYSTYRENE SULFONATE SODIUM POLYSTYRENE SULFONATE 454GM/BOT POWDER;ORAL, RECTAL Prescription No AA 204071 NUVO PHARMS INC

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