Tamiflu - 54868-6083-0 - (oseltamivir phosphate)

Alphabetical Index


Drug Information of Tamiflu

Product NDC: 54868-6083
Proprietary Name: Tamiflu
Non Proprietary Name: oseltamivir phosphate
Active Ingredient(s): 45    mg/1 & nbsp;   oseltamivir phosphate
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Tamiflu

Product NDC: 54868-6083
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021087
Marketing Category: NDA
Start Marketing Date: 20091030

Package Information of Tamiflu

Package NDC: 54868-6083-0
Package Description: 1 BLISTER PACK in 1 CARTON (54868-6083-0) > 10 CAPSULE in 1 BLISTER PACK

NDC Information of Tamiflu

NDC Code 54868-6083-0
Proprietary Name Tamiflu
Package Description 1 BLISTER PACK in 1 CARTON (54868-6083-0) > 10 CAPSULE in 1 BLISTER PACK
Product NDC 54868-6083
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name oseltamivir phosphate
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20091030
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name OSELTAMIVIR PHOSPHATE
Strength Number 45
Strength Unit mg/1
Pharmaceutical Classes Neuraminidase Inhibitor [EPC],Neuraminidase Inhibitors [MoA]

Complete Information of Tamiflu


General Information