Viramune - 0597-0047-24 - (nevirapine)

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Drug Information of Viramune

Product NDC: 0597-0047
Proprietary Name: Viramune
Non Proprietary Name: nevirapine
Active Ingredient(s): 50    mg/5mL & nbsp;   nevirapine
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Viramune

Product NDC: 0597-0047
Labeler Name: Boehringer Ingelheim Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020933
Marketing Category: NDA
Start Marketing Date: 20011001

Package Information of Viramune

Package NDC: 0597-0047-24
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (0597-0047-24) > 240 mL in 1 BOTTLE, PLASTIC

NDC Information of Viramune

NDC Code 0597-0047-24
Proprietary Name Viramune
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (0597-0047-24) > 240 mL in 1 BOTTLE, PLASTIC
Product NDC 0597-0047
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name nevirapine
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 20011001
Marketing Category Name NDA
Labeler Name Boehringer Ingelheim Pharmaceuticals Inc.
Substance Name NEVIRAPINE
Strength Number 50
Strength Unit mg/5mL
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 Viramune


General Information