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Azelastine Hydrochloride - 60505-0833-5 - (azelastine hydrochloride)

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Drug Information of Azelastine Hydrochloride

Product NDC: 60505-0833
Proprietary Name: Azelastine Hydrochloride
Non Proprietary Name: azelastine hydrochloride
Active Ingredient(s): 137    ug/1 & nbsp;   azelastine hydrochloride
Administration Route(s): NASAL
Dosage Form(s): SPRAY, METERED
Coding System: National Drug Codes(NDC)

Labeler Information of Azelastine Hydrochloride

Product NDC: 60505-0833
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077954
Marketing Category: ANDA
Start Marketing Date: 20100301

Package Information of Azelastine Hydrochloride

Package NDC: 60505-0833-5
Package Description: 1 BOTTLE, SPRAY in 1 CARTON (60505-0833-5) > 200 SPRAY, METERED in 1 BOTTLE, SPRAY

NDC Information of Azelastine Hydrochloride

NDC Code 60505-0833-5
Proprietary Name Azelastine Hydrochloride
Package Description 1 BOTTLE, SPRAY in 1 CARTON (60505-0833-5) > 200 SPRAY, METERED in 1 BOTTLE, SPRAY
Product NDC 60505-0833
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name azelastine hydrochloride
Dosage Form Name SPRAY, METERED
Route Name NASAL
Start Marketing Date 20100301
Marketing Category Name ANDA
Labeler Name Apotex Corp.
Substance Name AZELASTINE HYDROCHLORIDE
Strength Number 137
Strength Unit ug/1
Pharmaceutical Classes Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Inhibitor [EPC]

Complete Information of Azelastine Hydrochloride


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