Emtriva - 53808-0801-1 - (emtricitabine)

Alphabetical Index


Drug Information of Emtriva

Product NDC: 53808-0801
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: 53808-0801
Labeler Name: State of Florida DOH Central Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021500
Marketing Category: NDA
Start Marketing Date: 20090701

Package Information of Emtriva

Package NDC: 53808-0801-1
Package Description: 30 CAPSULE in 1 BLISTER PACK (53808-0801-1)

NDC Information of Emtriva

NDC Code 53808-0801-1
Proprietary Name Emtriva
Package Description 30 CAPSULE in 1 BLISTER PACK (53808-0801-1)
Product NDC 53808-0801
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name emtricitabine
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20090701
Marketing Category Name NDA
Labeler Name State of Florida DOH Central Pharmacy
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