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Epinastine Hydrochloride - 0574-4005-05 - (Epinastine Hydrochloride)

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Drug Information of Epinastine Hydrochloride

Product NDC: 0574-4005
Proprietary Name: Epinastine Hydrochloride
Non Proprietary Name: Epinastine Hydrochloride
Active Ingredient(s): .5    mg/mL & nbsp;   Epinastine Hydrochloride
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of Epinastine Hydrochloride

Product NDC: 0574-4005
Labeler Name: Paddock Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090951
Marketing Category: ANDA
Start Marketing Date: 20111101

Package Information of Epinastine Hydrochloride

Package NDC: 0574-4005-05
Package Description: 1 BOTTLE in 1 CARTON (0574-4005-05) > 5 mL in 1 BOTTLE

NDC Information of Epinastine Hydrochloride

NDC Code 0574-4005-05
Proprietary Name Epinastine Hydrochloride
Package Description 1 BOTTLE in 1 CARTON (0574-4005-05) > 5 mL in 1 BOTTLE
Product NDC 0574-4005
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Epinastine Hydrochloride
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 20111101
Marketing Category Name ANDA
Labeler Name Paddock Laboratories, Inc.
Substance Name EPINASTINE HYDROCHLORIDE
Strength Number .5
Strength Unit mg/mL
Pharmaceutical Classes Adrenergic Agonists [MoA],Adrenergic Receptor Agonist [EPC],Decreased Histamine Release [PE],Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Inhibitor [EPC]

Complete Information of Epinastine Hydrochloride


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