BEPREVE - 54868-6299-0 - (bepotastine besilate)

Alphabetical Index


Drug Information of BEPREVE

Product NDC: 54868-6299
Proprietary Name: BEPREVE
Non Proprietary Name: bepotastine besilate
Active Ingredient(s): 15    mg/mL & nbsp;   bepotastine besilate
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of BEPREVE

Product NDC: 54868-6299
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022288
Marketing Category: NDA
Start Marketing Date: 20110926

Package Information of BEPREVE

Package NDC: 54868-6299-0
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (54868-6299-0) > 10 mL in 1 BOTTLE, DROPPER

NDC Information of BEPREVE

NDC Code 54868-6299-0
Proprietary Name BEPREVE
Package Description 1 BOTTLE, DROPPER in 1 CARTON (54868-6299-0) > 10 mL in 1 BOTTLE, DROPPER
Product NDC 54868-6299
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name bepotastine besilate
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 20110926
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name BEPOTASTINE
Strength Number 15
Strength Unit mg/mL
Pharmaceutical Classes Histamine-1 Receptor Antagonist [EPC]

Complete Information of BEPREVE


General Information