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"71205-709-14" National Drug Code (NDC)
Cetirizine Hydrochloride 14 TABLET, FILM COATED in 1 BOTTLE (71205-709-14)
(Proficient Rx LP)
NDC Code
71205-709-14
Package Description
14 TABLET, FILM COATED in 1 BOTTLE (71205-709-14)
Product NDC
71205-709
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Cetirizine Hydrochloride
Non-Proprietary Name
Cetirizine Hydrochloride Tablets
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20181217
Marketing Category Name
ANDA
Application Number
ANDA078343
Manufacturer
Proficient Rx LP
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/71205-709-14