PATANOL - 54868-4528-0 - (olopatadine hydrochloride)

Alphabetical Index


Drug Information of PATANOL

Product NDC: 54868-4528
Proprietary Name: PATANOL
Non Proprietary Name: olopatadine hydrochloride
Active Ingredient(s): 1    mg/mL & nbsp;   olopatadine hydrochloride
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of PATANOL

Product NDC: 54868-4528
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020688
Marketing Category: NDA
Start Marketing Date: 20020508

Package Information of PATANOL

Package NDC: 54868-4528-0
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (54868-4528-0) > 5 mL in 1 BOTTLE, PLASTIC

NDC Information of PATANOL

NDC Code 54868-4528-0
Proprietary Name PATANOL
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (54868-4528-0) > 5 mL in 1 BOTTLE, PLASTIC
Product NDC 54868-4528
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name olopatadine hydrochloride
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 20020508
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name OLOPATADINE HYDROCHLORIDE
Strength Number 1
Strength Unit mg/mL
Pharmaceutical Classes Decreased Histamine Release [PE],Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Inhibitor [EPC]

Complete Information of PATANOL


General Information