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EPINASTINE HYDROCHLORIDE - 62756-329-90 - (EPINASTINE HYDROCHLORIDE)

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Drug Information of EPINASTINE HYDROCHLORIDE

Product NDC: 62756-329
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
Coding System: National Drug Codes(NDC)

Labeler Information of EPINASTINE HYDROCHLORIDE

Product NDC: 62756-329
Labeler Name: Sun Pharmaceutical Industries Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091626
Marketing Category: ANDA
Start Marketing Date: 20111101

Package Information of EPINASTINE HYDROCHLORIDE

Package NDC: 62756-329-90
Package Description: 1 BOTTLE in 1 CARTON (62756-329-90) > 5 mL in 1 BOTTLE

NDC Information of EPINASTINE HYDROCHLORIDE

NDC Code 62756-329-90
Proprietary Name EPINASTINE HYDROCHLORIDE
Package Description 1 BOTTLE in 1 CARTON (62756-329-90) > 5 mL in 1 BOTTLE
Product NDC 62756-329
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name EPINASTINE HYDROCHLORIDE
Dosage Form Name SOLUTION
Route Name OPHTHALMIC
Start Marketing Date 20111101
Marketing Category Name ANDA
Labeler Name Sun Pharmaceutical Industries Limited
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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