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"21695-709-14" National Drug Code (NDC)
Cetirizine Hydrochloride 14 TABLET in 1 BOTTLE (21695-709-14)
(Rebel Distributors Corp)
NDC Code
21695-709-14
Package Description
14 TABLET in 1 BOTTLE (21695-709-14)
Product NDC
21695-709
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Cetirizine Hydrochloride
Non-Proprietary Name
Cetirizine Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20071227
Marketing Category Name
ANDA
Application Number
ANDA077946
Manufacturer
Rebel Distributors Corp
Substance Name
CETIRIZINE HYDROCHLORIDE
Strength
10
Strength Unit
mg/1
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/21695-709-14