Efavirenz

Product NDC
42543-889
11-digit product format
425430889
Labeler code
42543
Product ID
42543-889_2eb82d5c-feff-413e-9966-ab5498ae86bf
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Efavirenz
Dosage form
TABLET
Route
ORAL
Labeler
Strides Pharma Inc.
Application
ANDA204869
Marketing category
ANDA
Marketing start
2021-01-11
Marketing end
0000-00-00
Substance
EFAVIRENZ
Active strength
600 mg/1
Pharmacologic classes
Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Non-Nucleoside Analog [EXT],Non-Nucleoside Reverse Transcriptase Inhibitors [MoA],Cytochrome P450 3A Inducers [MoA],Cytochrome P450 2B6 Inducers [MoA],Cytochrome P450 2C9 Inhibitors [MoA],Cytochrome P450 2C19 Inhibitors [MoA],Cytochrome P450 3A4 Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
42543-889-04EA - Each42543-8897983f543-3d87-4fb8-b44e-53a0bd70565312021-01-08

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
42543-889-044254308890430 TABLET in 1 BOTTLE (42543-889-04) 30 tablet2021-01-110000-00-00NoNoCurrent