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"30142-571-22" National Drug Code (NDC)
Fexo Fenadine 3 BLISTER PACK in 1 CARTON (30142-571-22) > 5 TABLET, FILM COATED in 1 BLISTER PACK
(Kroger Company)
NDC Code
30142-571-22
Package Description
3 BLISTER PACK in 1 CARTON (30142-571-22) > 5 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC
30142-571
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Fexo Fenadine
Non-Proprietary Name
Fexofenadine Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20110416
Marketing Category Name
ANDA
Application Number
ANDA076447
Manufacturer
Kroger Company
Substance Name
FEXOFENADINE HYDROCHLORIDE
Strength
180
Strength Unit
mg/1
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/30142-571-22