Tamiflu - 54868-6315-0 - (Oseltamivir Phosphate)

Alphabetical Index


Drug Information of Tamiflu

Product NDC: 54868-6315
Proprietary Name: Tamiflu
Non Proprietary Name: Oseltamivir Phosphate
Active Ingredient(s): 6    mg/mL & nbsp;   Oseltamivir Phosphate
Administration Route(s): ORAL
Dosage Form(s): POWDER, FOR SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Tamiflu

Product NDC: 54868-6315
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021246
Marketing Category: NDA
Start Marketing Date: 20111103

Package Information of Tamiflu

Package NDC: 54868-6315-0
Package Description: 1 BOTTLE, GLASS in 1 CARTON (54868-6315-0) > 6 mL in 1 BOTTLE, GLASS

NDC Information of Tamiflu

NDC Code 54868-6315-0
Proprietary Name Tamiflu
Package Description 1 BOTTLE, GLASS in 1 CARTON (54868-6315-0) > 6 mL in 1 BOTTLE, GLASS
Product NDC 54868-6315
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oseltamivir Phosphate
Dosage Form Name POWDER, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 20111103
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name OSELTAMIVIR PHOSPHATE
Strength Number 6
Strength Unit mg/mL
Pharmaceutical Classes Neuraminidase Inhibitor [EPC],Neuraminidase Inhibitors [MoA]

Complete Information of Tamiflu


General Information