Prandin - 54868-5381-2 - (repaglinide)

Alphabetical Index


Drug Information of Prandin

Product NDC: 54868-5381
Proprietary Name: Prandin
Non Proprietary Name: repaglinide
Active Ingredient(s): 2    mg/1 & nbsp;   repaglinide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Prandin

Product NDC: 54868-5381
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020741
Marketing Category: NDA
Start Marketing Date: 20050808

Package Information of Prandin

Package NDC: 54868-5381-2
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC (54868-5381-2)

NDC Information of Prandin

NDC Code 54868-5381-2
Proprietary Name Prandin
Package Description 60 TABLET in 1 BOTTLE, PLASTIC (54868-5381-2)
Product NDC 54868-5381
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name repaglinide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20050808
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name REPAGLINIDE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Glinide [EPC],Potassium Channel Antagonists [MoA]

Complete Information of Prandin


General Information