Nevirapine - 0378-4050-80 - (nevirapine)

Alphabetical Index


Drug Information of Nevirapine

Product NDC: 0378-4050
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: 0378-4050
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202523
Marketing Category: ANDA
Start Marketing Date: 20120522

Package Information of Nevirapine

Package NDC: 0378-4050-80
Package Description: 180 TABLET in 1 BOTTLE, PLASTIC (0378-4050-80)

NDC Information of Nevirapine

NDC Code 0378-4050-80
Proprietary Name Nevirapine
Package Description 180 TABLET in 1 BOTTLE, PLASTIC (0378-4050-80)
Product NDC 0378-4050
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 Mylan Pharmaceuticals Inc.
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