FDA.reportPublic FDA data

Tri Femynor

Product NDC
50090-3239
11-digit product format
500903239
Labeler code
50090
Product ID
50090-3239_c6c36c75-48a8-43b9-9b8c-ee40d3591ccd
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
norgestimate and ethinyl estradiol
Dosage form
KIT
Labeler
A-S Medication Solutions
Application
ANDA203870
Marketing category
ANDA
Marketing start
2016-10-28
Marketing end
0000-00-00
Active strength
0
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
50090-3239-02023-02-06C16284748780-1f386c649-b83f-0266-e053-dadaa90a7c1a0b33e837-a6b5-4dc9-8097-ad3d3cd7e50f
50090-3239-02023-01-30C16284748780-1f386c649-b83f-0266-e053-dadaa90a7c1a0b33e837-a6b5-4dc9-8097-ad3d3cd7e50f

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-3239-0EA - Each50090-32394a57d206-494b-467c-94df-4acb9f4b61fa12019-05-02

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50090-3239-0500903239001 KIT in 1 KIT (50090-3239-0) 1 kit2017-11-020000-00-00NoNoCurrent