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Serving leading biopharmaceutical companies globally:

Chinese Patent Office
Medtronic
Johnson and Johnson
Dow
Express Scripts
UBS
Boehringer Ingelheim
QuintilesIMS
Argus Health
Queensland Health

Generated: February 22, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 202333

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NDA 202333 describes SODIUM POLYSTYRENE SULFONATE, which is a drug marketed by Ailex Pharms Llc, Belcher Pharms Llc, Citrusphrma, Cmp Pharma Inc, Eci Pharms Llc, Epic Pharma Llc, Nuvo Pharm Inc, Wockhardt, Morton Grove, Paddock Llc, Roxane, and West-ward Pharms Int, and is included in twelve NDAs. It is available from eleven suppliers. Additional details are available on the SODIUM POLYSTYRENE SULFONATE profile page.

The generic ingredient in SODIUM POLYSTYRENE SULFONATE is sodium polystyrene sulfonate. There are one thousand four hundred and fifteen drug master file entries for this compound. Eighteen suppliers are listed for this compound. Additional details are available on the sodium polystyrene sulfonate profile page.
Summary for 202333
Tradename:SODIUM POLYSTYRENE SULFONATE
Applicant:Epic Pharma Llc
Ingredient:sodium polystyrene sulfonate
Patents:0
Therapeutic Class:Antidotes, Deterrents, and Toxicologic Agents
Formulation / Manufacturing:see details
Suppliers and Packaging for NDA: 202333
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
SODIUM POLYSTYRENE SULFONATE sodium polystyrene sulfonate POWDER;ORAL, RECTAL 202333 ANDA PuraCap Laboratories LLC dba Blu Pharmaceuticals 24658-760 N 24658-760-16
SODIUM POLYSTYRENE SULFONATE sodium polystyrene sulfonate POWDER;ORAL, RECTAL 202333 ANDA Epic Pharma, LLC 42806-013 N 42806-013-96

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:POWDER;ORAL, RECTALStrength453.6GM/BOT
Approval Date:Mar 19, 2014TE:AARLD:No

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Colorcon
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Merck
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Cantor Fitzgerald
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