Nevirapine - 31722-505-10 - (Nevirapine)

Alphabetical Index


Drug Information of Nevirapine

Product NDC: 31722-505
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: 31722-505
Labeler Name: Camber Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078584
Marketing Category: ANDA
Start Marketing Date: 20120523

Package Information of Nevirapine

Package NDC: 31722-505-10
Package Description: 1000 TABLET in 1 BOTTLE (31722-505-10)

NDC Information of Nevirapine

NDC Code 31722-505-10
Proprietary Name Nevirapine
Package Description 1000 TABLET in 1 BOTTLE (31722-505-10)
Product NDC 31722-505
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nevirapine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120523
Marketing Category Name ANDA
Labeler Name Camber 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