Nevirapine - 65862-027-10 - (Nevirapine)

Alphabetical Index


Drug Information of Nevirapine

Product NDC: 65862-027
Proprietary Name: Nevirapine
Non Proprietary Name: Nevirapine
Active Ingredient(s): 200    mg/1 & nbsp;   Nevirapine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Nevirapine

Product NDC: 65862-027
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077521
Marketing Category: ANDA
Start Marketing Date: 20120522

Package Information of Nevirapine

Package NDC: 65862-027-10
Package Description: 6 BLISTER PACK in 1 CARTON (65862-027-10) > 10 TABLET in 1 BLISTER PACK

NDC Information of Nevirapine

NDC Code 65862-027-10
Proprietary Name Nevirapine
Package Description 6 BLISTER PACK in 1 CARTON (65862-027-10) > 10 TABLET in 1 BLISTER PACK
Product NDC 65862-027
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nevirapine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120522
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name NEVIRAPINE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Non-Nucleoside Analog [Chemical/Ingredient],Non-Nucleoside Reverse Transcriptase Inhibitors [MoA]

Complete Information of Nevirapine


General Information