etravirine

Product NDC
69238-1720
11-digit product format
692381720
Labeler code
69238
Product ID
69238-1720_2ea1c501-299b-4bea-97d6-d0c695d58271
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
etravirine
Dosage form
TABLET
Route
ORAL
Labeler
Amneal Pharmaceuticals NY LLC
Application
ANDA214196
Marketing category
ANDA
Marketing start
2021-06-14
Marketing end
0000-00-00
Substance
ETRAVIRINE
Active strength
25 mg/1
Pharmacologic classes
Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 2C9 Inhibitors [MoA], Cytochrome P450 3A Inducers [MoA], Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Non-Nucleoside Analog [EXT], Non-Nucleoside Reverse Transcriptase Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
08bcdf9c-0f44-79ee-51ca-e7f77478ea2eProduct name220230112

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69238-1720ETRAVIRINE TABLET [AMNEAL PHARMACEUTICALS NY LLC]2Legacy NDC20231231_f6430b98-b521-46e5-af98-b1d9b128d1f9.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69238-1720-769238172007120 TABLET in 1 BOTTLE, PLASTIC (69238-1720-7) 120 tablet2021-06-140000-00-00NoNoCurrent