Bepreve - 24208-629-01 - (bepotastine besilate)

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Drug Information of Bepreve

Product NDC: 24208-629
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: 24208-629
Labeler Name: Bausch & Lomb Incorporated
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022288
Marketing Category: NDA
Start Marketing Date: 20090908

Package Information of Bepreve

Package NDC: 24208-629-01
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (24208-629-01) > 10 mL in 1 BOTTLE, DROPPER

NDC Information of Bepreve

NDC Code 24208-629-01
Proprietary Name Bepreve
Package Description 1 BOTTLE, DROPPER in 1 CARTON (24208-629-01) > 10 mL in 1 BOTTLE, DROPPER
Product NDC 24208-629
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name bepotastine besilate
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 20090908
Marketing Category Name NDA
Labeler Name Bausch & Lomb Incorporated
Substance Name BEPOTASTINE BESILATE
Strength Number 15
Strength Unit mg/mL
Pharmaceutical Classes Histamine-1 Receptor Antagonist [EPC]

Complete Information of Bepreve


General Information