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"49349-890-02" National Drug Code (NDC)
Fexofenadine Hydrochloride 30 TABLET, FILM COATED in 1 BLISTER PACK (49349-890-02)
(REMEDYREPACK INC.)
NDC Code
49349-890-02
Package Description
30 TABLET, FILM COATED in 1 BLISTER PACK (49349-890-02)
Product NDC
49349-890
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Fexofenadine Hydrochloride
Non-Proprietary Name
Fexofenadine Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20151026
Marketing Category Name
ANDA
Application Number
ANDA076447
Manufacturer
REMEDYREPACK INC.
Substance Name
FEXOFENADINE HYDROCHLORIDE
Strength
180
Strength Unit
mg/1
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/49349-890-02