Emtriva - 54868-4853-0 - (emtricitabine)

Alphabetical Index


Drug Information of Emtriva

Product NDC: 54868-4853
Proprietary Name: Emtriva
Non Proprietary Name: emtricitabine
Active Ingredient(s): 200    mg/1 & nbsp;   emtricitabine
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Emtriva

Product NDC: 54868-4853
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021500
Marketing Category: NDA
Start Marketing Date: 20030710

Package Information of Emtriva

Package NDC: 54868-4853-0
Package Description: 30 CAPSULE in 1 BOTTLE, PLASTIC (54868-4853-0)

NDC Information of Emtriva

NDC Code 54868-4853-0
Proprietary Name Emtriva
Package Description 30 CAPSULE in 1 BOTTLE, PLASTIC (54868-4853-0)
Product NDC 54868-4853
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name emtricitabine
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20030710
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name EMTRICITABINE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient],Nucleoside Reverse Transcriptase Inhibitors [MoA]

Complete Information of Emtriva


General Information