NEVIRAPINE

Product NDC

69097-403

11-digit product format

690970403

Labeler code

69097

Product ID

69097-403_def35264-15cf-4def-8558-c80af302b018

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

NEVIRAPINE

Dosage form

TABLET, EXTENDED RELEASE

Route

ORAL

Labeler

Cipla USA Inc.

Application

ANDA206448

Marketing category

ANDA

Marketing start

2015-10-15

Marketing end

2019-12-31

Substance

NEVIRAPINE

Active strength

400 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]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record