E-Z Prep, E-Z Prep 220

NDA 19382, held by Clinipad. Povidone-Iodine.

As of Nov 14, 2026, NDA 19382 (E-Z Prep, E-Z Prep 220), held by Clinipad, was first approved by FDA on Jul 25, 1989, with 1 approved supplement and 0 published complete response letters.

First approved: Jul 25, 1989
Review: Standard
Supplements approved: 1
Complete response letters: 0

Approvals and New Uses

The original application and every efficacy supplement, newest first; all 2 submissions below

Date	Submission	Status	Documents
Jul 25, 1989	Original applicationNew dosage form · Standard review	Approved	None posted

Products

3 strengths and forms


E-Z Prep10% · solution;topical	Povidone-Iodine	Discontinued
E-Z Prep5% · sponge;topical	Povidone-Iodine	Discontinued
E-Z Prep 2205% · sponge;topical	Povidone-Iodine	Discontinued

All 2 submissions, including labeling and manufacturing supplements


Sep 10, 1998	Supplement 1Manufacturing · Standard review	Approved	None posted
Jul 25, 1989	Original applicationNew dosage form · Standard review	Approved	None posted

Identifiers

Application: NDA 19382
Drugs@FDA: Overview at FDA
Company: Clinipad

Approvals, supplements, products and documents come from FDA's Drugs@FDA data files, refreshed daily; Drugs@FDA lists approved applications only. Complete response letters are FDA's published letters. Drugs@FDA and FDA complete response letters