Efavirenz

Product NDC
65862-774
11-digit product format
658620774
Labeler code
65862
Product ID
65862-774_eba5118d-9e41-40bc-87bc-e2a61ff044a0
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Efavirenz
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Aurobindo Pharma Limited
Application
ANDA205322
Marketing category
ANDA
Marketing start
2018-08-30
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
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
65862-774-30EA - Each65862-774807a1e3b-e51f-4a31-9df2-8b4f098ebdc012018-11-06

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
65862-774-306586207743030 TABLET, FILM COATED in 1 BOTTLE (65862-774-30) 2018-08-300000-00-00NoNoCurrent