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"61919-429-30" National Drug Code (NDC)
Cetirizine Hydrochloride 30 TABLET in 1 BOTTLE (61919-429-30)
(DIRECT RX)
NDC Code
61919-429-30
Package Description
30 TABLET in 1 BOTTLE (61919-429-30)
Product NDC
61919-429
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Cetirizine Hydrochloride
Non-Proprietary Name
Cetirizine Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20161222
Marketing Category Name
ANDA
Application Number
ANDA077829
Manufacturer
DIRECT RX
Substance Name
CETIRIZINE HYDROCHLORIDE
Strength
10
Strength Unit
mg/1
Pharmacy Classes
Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61919-429-30