FDA.reportPublic FDA data

PROVIDONE-IODINE PREP PADS

Product NDC
72766-005
Requested package NDC
72766-005-01
11-digit product format
727660005
Labeler code
72766
Product ID
72766-005_e5ed44c0-b764-77c4-e053-2995a90af3e3
Type
HUMAN OTC DRUG
Nonproprietary name
POVIDONE-IODINE PREP PADS
Dosage form
SWAB
Route
TOPICAL
Labeler
Yangzhou Suxiang Medical Instrument Co, LTD
Application
part333A
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2022-08-31
Marketing end
0000-00-00
Substance
POVIDONE-IODINE
Active strength
0 g/1
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage72766-00572766-005-01DDiscontinued by firm2026-07-31

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
72766-005-01727660005011 SWAB in 1 PACKET (72766-005-01) 1 swab2022-08-310000-00-00NoNoCurrent