FDA.reportPublic FDA data

Diclotrex

Product NDC
59088-716
11-digit product format
590880716
Labeler code
59088
Product ID
59088-716_d1022c1b-bb3c-1c0d-e053-2995a90aeac4
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
diclofenac sodium, camphor, menthol
Dosage form
KIT
Route
TOPICAL
Labeler
PureTek Corporation
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2018-10-23
Marketing end
2028-10-19
Active strength
0
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
59088-716-00EA - Each59088-71645dc7c7d-0199-48cd-bb32-29b84f724a7112020-09-14

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
59088-716-00590880716001 KIT in 1 KIT (59088-716-00) * 1 CARTON in 1 KIT > 1 BOTTLE in 1 CARTON (59088-372-10) > 150 mL in 1 BOTTLE * 85 g in 1 BOTTLE, WITH APPLICATOR (59088-283-07) 1 kit2018-10-230000-00-00NoNoCurrent