SELENIUM SULFIDE

Product NDC
68071-1768
11-digit product format
680711768
Labeler code
68071
Product ID
68071-1768_c46d2f34-29cb-11fc-e053-2a95a90a84ab
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
SELENIUM SULFIDE
Dosage form
LOTION
Route
TOPICAL
Labeler
NuCare Pharmaceuticals,Inc.
Application
ANDA089996
Marketing category
ANDA
Marketing start
2006-09-25
Marketing end
0000-00-00
Substance
SELENIUM SULFIDE
Active strength
3 mg/100mL
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68071-1768-42023-01-30C16284748780-1f386c64a-2366-0266-e053-dadaa90a7c1aSelenium Sulfide Topical Suspension USP, 2.5% (Lotion)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68071-1768-4SELENIUM SULFIDE118 mL in 1 BOTTLELOTION1181

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68071-1768SELENIUM SULFIDE LOTION [NUCARE PHARMACEUTICALS,INC.]1Legacy NDC, 1 package rows20210611_c46d25b5-d2db-61a3-e053-2a95a90a86d7.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68071-1768-468071176804118 mL in 1 BOTTLE (68071-1768-4) 118 ml2021-06-100000-00-00NoNoCurrent