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"47335-938-90" National Drug Code (NDC)
Azelastine Hydrochloride 1 BOTTLE, PLASTIC in 1 BOX (47335-938-90) > 6 mL in 1 BOTTLE, PLASTIC
(Sun Pharmaceutical Industries, Inc.)
NDC Code
47335-938-90
Package Description
1 BOTTLE, PLASTIC in 1 BOX (47335-938-90) > 6 mL in 1 BOTTLE, PLASTIC
Product NDC
47335-938
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Azelastine Hydrochloride
Non-Proprietary Name
Azelastine Hydrochloride
Dosage Form
SOLUTION/ DROPS
Usage
INTRAOCULAR
Start Marketing Date
20100531
Marketing Category Name
ANDA
Application Number
ANDA078738
Manufacturer
Sun Pharmaceutical Industries, Inc.
Substance Name
AZELASTINE HYDROCHLORIDE
Strength
.5
Strength Unit
mg/mL
Pharmacy Classes
Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/47335-938-90