Nevirapine

Basic Information

Product Name

Nevirapine

FDA Product Code

33342-004

Regulatory Information

NDC Product Code

33342-004

Application Number

ANDA090688

Marketing Category

C73584

Effective Date

August 16, 2023

Territorial Authority

USA

FDA Title

These highlights do not include all the information needed to use NEVIRAPINE TABLETS safely and effectively. See full prescribing information for NEVIRAPINE TABLETS. NEVIRAPINE tablets, for oral use Initial U.S. Approval: 1996

Labeling Type

Human Prescription Drug Label

Version Number

Active Ingredients

NEVIRAPINE

Quantity: 200 mg in 1 1

Code: 99DK7FVK1H

Class Code: ACTIB

CELLULOSE, MICROCRYSTALLINE

Code: OP1R32D61U

Class Code: IACT

LACTOSE MONOHYDRATE

Code: EWQ57Q8I5X

Class Code: IACT

POVIDONE

Code: FZ989GH94E

Class Code: IACT

SODIUM STARCH GLYCOLATE TYPE A POTATO

Code: 5856J3G2A2

Class Code: IACT

SILICON DIOXIDE

Code: ETJ7Z6XBU4

Class Code: IACT

MAGNESIUM STEARATE

Code: 70097M6I30

Class Code: IACT

Active Moieties

Code: 99DK7FVK1H

Nevirapine

Basic Information

Regulatory Information

Company Information

Active Ingredients

CELLULOSE, MICROCRYSTALLINE

LACTOSE MONOHYDRATE

POVIDONE

SODIUM STARCH GLYCOLATE TYPE A POTATO

SILICON DIOXIDE

MAGNESIUM STEARATE

Active Moieties

NEVIRAPINE